Missa Bay of New Jersey is recalling close to 300,000 cases of sliced apples due to a positive finding of Listeria monocytogenes on the processing equipment used to process the sliced apples. Product was shipped to 36 states and the District of Columbia. There have been no reported illnesses.
At the time of this release, the potential pathogen was found on processing equipment, most likely a food contact surface. One would guess that extensive testing is being completed to see if there are product positive samples.
Historically, fruits were considered low risk because of their acidic nature. But sliced fruit products such as tomatoes, apples and melons, at the least, will support survival, and if conditions are right, can support growth of Listeria. In a study by Conway etal (link below), Listeria did grow on apple slices when those slices were stored at temperatures above refrigeration temperature. Two issues here would be that product is often purchased for children, and the potential for storage at elevated temperatures by the consumer.
FDA Recall News Release
Missa Bay, LLC Announces Voluntary Recall Of Fruit, Vegetable, and Sandwich Products Containing Apples Because of Possible Health Risk
http://www.fda.gov/Safety/Recalls/ucm315249.htm
Contact
Consumer
1‐800‐800‐7822
Media
Tristan Simpson
Corporate Communications
626‐678‐2055
FOR IMMEDIATE RELEASE - August 10, 2012 - Missa Bay, LLC, a wholly owned subsidiary of Ready Pac Foods, Inc., of Swedesboro, New Jersey is voluntarily recalling a total of 293,488 cases and 296,224 individually distributed units of fruit, vegetable, and sandwich products containing apples, as listed below, with the Use‐by dates of July 8, 2012 through August 20, 2012 because they contain diced or sliced apples which may be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism that can cause serious or life‐threatening food borne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastro intestinal symptoms such as nausea or diarrhea. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.
The recalled products were produced and distributed from the Missa Bay, LLC facility to retailers and foodservice operators in the following states: Alabama, Arkansas, Connecticut, Delaware, District of Columbia, Washington D.C., Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Mississippi, Montana, Nebraska, New Hampshire, New Jersey, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Vermont, Virginia, Wisconsin and West Virginia.
Monday, August 13, 2012
Burch Equipment of NC Expands Cantaloupe Recall and Now Includes Honeydew Melons
Burch Equipment of North Carolina is now recalling all of this season's cantaloupes and honeydew melons due to possible contamination with Listeria monocytogenes. On August 5th, they issued a recall for melons, (http://pennstatefoodsafety.blogspot.com/2012/08/nc-company-recalls-cantaloupes-due-to.html), but this expansion was based upon a positive finding of Listeria monocytogens on honeydew melon grown and packed by Burch.
There have been no reported illnesses. According to the release, product was shipped to at least 18 states:
Unfortunately, this scenario is similar to others in that a positive test for Listeria causes an initial recall. After the regulatory agencies evaluate and test, the recall is expanded due to the fact that Listeria, a pathogen present in plant environments, was not under control, and thus was not limited to that lot initially recalled.
FDA News Release
Recall -- Firm Press Release
http://www.fda.gov/Safety/Recalls/ucm315248.htm?source=govdelivery
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Burch Equipment LLC Expands Recall to Include Additional Cantaloupe Shipping Dates and to include Honeydew Melons
Contact
Consumer:
910-267-5781
burch@intrstar.net
FOR IMMEDIATE RELEASE - August 10, 2012 - Burch Equipment LLC, North Carolina, is expanding its recall to include all of this growing season's cantaloupes and honeydew melons that may remain on the market because they may possibly be contaminated with Listeria monocytogenes. There have been no illnesses reported to date.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, infection can cause miscarriages and stillbirths among pregnant women. The incubation period (the length of time between consuming a product and becoming ill) for Listeria monocytogenes can be 1 to 3 weeks, but may be in the range of 3 to 70 days.
The whole cantaloupes are identified by a red label reading Burch Farms referencing PLU # 4319. All cantaloupes involved in the recall were grown by Burch Farms, however some of the cantaloupes may have been identified with a "Cottle Strawberry, Inc." sticker referencing PLU #4319 (note: Cottle Strawberry, Inc. did not grow or process the cantaloupe involved in this recall). Cantaloupes from Burch Farms were shipped in both corrugated boxes (9 cantaloupe per case) and in bulk bins.
Honeydew melons involved in this recall expansion do not bear any identifying stickers and were packed in cartons labeled melons.
Consumers who may have purchased these honeydew melons should contact the store where they purchased their melons, for information about whether those melons are part of this recall.
The cantaloupes and honeydew melons involved in this expanded recall were sold to distributors between June 23rd and July 27th, in the following states: FL, GA, IL, KY, MA, MD, ME, MI, NC, NH, NJ, NY, OH, PA, SC, and VA, VT and WV. The melons may have further been distributed to retail stores, restaurants and food service facilities in other states."
Burch Equipment LLC is requesting any consumer that may have one of these cantaloupes or honeydews to discard the product.
There have been no illnesses reported to date. FDA and the North Carolina Department of Agriculture and Consumer Services are working with Burch Equipment LLC following a random sample of a cantaloupe testing positive for Listeria monocytogenes.
This recall expansion is based on FDA's finding of Listeria monocytogenes on a honeydew melon grown and packed by Burch..
Burch Farms lacked audits, traceability on recalled fruit
http://www.thepacker.com/fruit-vegetable-news/Burch-Farms-lacked-audits-traceability-on-recalled-fruit-166458376.html
08/16/2012 3:48:34 PM
Coral Beach
Listeria contamination has been confirmed at the Burch Farms melon packing facility in Faison, N.C., according to the Food and Drug Administration.
In an update posted on its website late Aug. 13, FDA officials said the listeria finding spurred Burch to expand its recall to include all cantaloupe and honeydew melons shipped this season. No illnesses have been reported in relation to the recalled melons.
“This recall expansion is based on the FDA’s finding of Listeria monocytogenes (L. mono) on a honeydew melon grown and packed by Burch Farms. The recall expansion is also a result of the agency’s finding of L. mono in the environment of the firm’s packing facility,” according to the notice.
Company spokeswoman Teresa Burch said it has not had its cantaloupe operation audited by a third party for food safety practices, and although the company has traceability programs for other items, there is none in place for its melons.
Burch Equipment LLC, doing business as Burch Farms, originally recalled about 5,200 cantaloupes July 28 after the U.S. Department of Agriculture’s Microbiological Data Program found listeria on one melon at retail during a random sampling.
The grower expanded the recall to include 188,900 cantaloupes Aug. 3 and corrected the variety from athena to caribbean golds. That expansion came after the FDA revealed it had found “unsanitary conditions” at the Burch packing shed.
Owner Jimmy Burch Sr. said Aug. 14 that investigators had just left his farm that morning.
“I asked the guy who took the samples and he said he couldn’t tell me anything,” Burch said. “They just said ‘you’ll be getting results in a few days’ and left.”
Burch said he uses the sanitizer SaniDate in his packing facility’s water. According to the Burch Farms website, the operations are audited by PrimusLabs.
PrimusLabs in-house counsel Ryan Fothergill confirmed that the company has audited the leafy greens processing and field operations at Burch Farms but not the cantaloupe operation. Fothergill said Primus records show its staff was last at the Burch operation in March.
Burch said he planted only about 10 acres of honeydews for this season. The entire crop went to wholesalers. He said his farm has not had food safety issues in the past.
“We shipped 3,000 loads of produce last year with no problems,” Burch said.
According to Burch and the FDA, the recalled honeydews do not have any identifying stickers. They were packed in cartons labeled “melons.”
In its latest recall notice the company reminded consumers that the listeria incubation period “can be one to three weeks, but may be in the range of three to 70 days.”
Complete distribution details on the melons are not available, according to the FDA.
The Burch cantaloupes and honeydew melons were sold to distributors from June 23 to July 27, in Florida, Georgia, Illinois, Kentucky, Massachusetts, Maryland, Maine, Michigan, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, South Carolina, and Virginia, Vermont and West Virginia, the Aug. 10 recall states.
“The melons may have further been distributed to retail stores, restaurants and food service facilities in other states,” according to the recall.
There have been no reported illnesses. According to the release, product was shipped to at least 18 states:
"The cantaloupes and honeydew melons involved in this expanded recall were sold to distributors between June 23rd and July 27th, in the following states: FL, GA, IL, KY, MA, MD, ME, MI, NC, NH, NJ, NY, OH, PA, SC, and VA, VT and WV. The melons may have further been distributed to retail stores, restaurants and food service facilities in other states."
Unfortunately, this scenario is similar to others in that a positive test for Listeria causes an initial recall. After the regulatory agencies evaluate and test, the recall is expanded due to the fact that Listeria, a pathogen present in plant environments, was not under control, and thus was not limited to that lot initially recalled.
FDA News Release
Recall -- Firm Press Release
http://www.fda.gov/Safety/Recalls/ucm315248.htm?source=govdelivery
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Burch Equipment LLC Expands Recall to Include Additional Cantaloupe Shipping Dates and to include Honeydew Melons
Contact
Consumer:
910-267-5781
burch@intrstar.net
FOR IMMEDIATE RELEASE - August 10, 2012 - Burch Equipment LLC, North Carolina, is expanding its recall to include all of this growing season's cantaloupes and honeydew melons that may remain on the market because they may possibly be contaminated with Listeria monocytogenes. There have been no illnesses reported to date.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, infection can cause miscarriages and stillbirths among pregnant women. The incubation period (the length of time between consuming a product and becoming ill) for Listeria monocytogenes can be 1 to 3 weeks, but may be in the range of 3 to 70 days.
The whole cantaloupes are identified by a red label reading Burch Farms referencing PLU # 4319. All cantaloupes involved in the recall were grown by Burch Farms, however some of the cantaloupes may have been identified with a "Cottle Strawberry, Inc." sticker referencing PLU #4319 (note: Cottle Strawberry, Inc. did not grow or process the cantaloupe involved in this recall). Cantaloupes from Burch Farms were shipped in both corrugated boxes (9 cantaloupe per case) and in bulk bins.
Honeydew melons involved in this recall expansion do not bear any identifying stickers and were packed in cartons labeled melons.
Consumers who may have purchased these honeydew melons should contact the store where they purchased their melons, for information about whether those melons are part of this recall.
The cantaloupes and honeydew melons involved in this expanded recall were sold to distributors between June 23rd and July 27th, in the following states: FL, GA, IL, KY, MA, MD, ME, MI, NC, NH, NJ, NY, OH, PA, SC, and VA, VT and WV. The melons may have further been distributed to retail stores, restaurants and food service facilities in other states."
Burch Equipment LLC is requesting any consumer that may have one of these cantaloupes or honeydews to discard the product.
There have been no illnesses reported to date. FDA and the North Carolina Department of Agriculture and Consumer Services are working with Burch Equipment LLC following a random sample of a cantaloupe testing positive for Listeria monocytogenes.
This recall expansion is based on FDA's finding of Listeria monocytogenes on a honeydew melon grown and packed by Burch..
Burch Farms lacked audits, traceability on recalled fruit
http://www.thepacker.com/fruit-vegetable-news/Burch-Farms-lacked-audits-traceability-on-recalled-fruit-166458376.html
08/16/2012 3:48:34 PM
Coral Beach
Listeria contamination has been confirmed at the Burch Farms melon packing facility in Faison, N.C., according to the Food and Drug Administration.
In an update posted on its website late Aug. 13, FDA officials said the listeria finding spurred Burch to expand its recall to include all cantaloupe and honeydew melons shipped this season. No illnesses have been reported in relation to the recalled melons.
“This recall expansion is based on the FDA’s finding of Listeria monocytogenes (L. mono) on a honeydew melon grown and packed by Burch Farms. The recall expansion is also a result of the agency’s finding of L. mono in the environment of the firm’s packing facility,” according to the notice.
Company spokeswoman Teresa Burch said it has not had its cantaloupe operation audited by a third party for food safety practices, and although the company has traceability programs for other items, there is none in place for its melons.
Burch Equipment LLC, doing business as Burch Farms, originally recalled about 5,200 cantaloupes July 28 after the U.S. Department of Agriculture’s Microbiological Data Program found listeria on one melon at retail during a random sampling.
The grower expanded the recall to include 188,900 cantaloupes Aug. 3 and corrected the variety from athena to caribbean golds. That expansion came after the FDA revealed it had found “unsanitary conditions” at the Burch packing shed.
Owner Jimmy Burch Sr. said Aug. 14 that investigators had just left his farm that morning.
“I asked the guy who took the samples and he said he couldn’t tell me anything,” Burch said. “They just said ‘you’ll be getting results in a few days’ and left.”
Burch said he uses the sanitizer SaniDate in his packing facility’s water. According to the Burch Farms website, the operations are audited by PrimusLabs.
PrimusLabs in-house counsel Ryan Fothergill confirmed that the company has audited the leafy greens processing and field operations at Burch Farms but not the cantaloupe operation. Fothergill said Primus records show its staff was last at the Burch operation in March.
Burch said he planted only about 10 acres of honeydews for this season. The entire crop went to wholesalers. He said his farm has not had food safety issues in the past.
“We shipped 3,000 loads of produce last year with no problems,” Burch said.
According to Burch and the FDA, the recalled honeydews do not have any identifying stickers. They were packed in cartons labeled “melons.”
In its latest recall notice the company reminded consumers that the listeria incubation period “can be one to three weeks, but may be in the range of three to 70 days.”
Complete distribution details on the melons are not available, according to the FDA.
The Burch cantaloupes and honeydew melons were sold to distributors from June 23 to July 27, in Florida, Georgia, Illinois, Kentucky, Massachusetts, Maryland, Maine, Michigan, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, South Carolina, and Virginia, Vermont and West Virginia, the Aug. 10 recall states.
“The melons may have further been distributed to retail stores, restaurants and food service facilities in other states,” according to the recall.
Friday, August 10, 2012
Grape Tomatoes and Cilantro Recalled After Testing Positive for Salmonella
Grape tomatoes and cilantro are being recalled after product tested positive for Salmonella. Both were conducted by the Minnesota Dept of Ag. There have been no reported illnesses. Distibution of tomatoes amd cilantro were limited to MN, WI, and MI
Menno Beachy Recalls Grape Tomatoes Because Of Possible Health Risk
Limited Distribution In Minnesota, Wisconsin, And Michiganhttp://www.fda.gov/Safety/Recalls/ucm314871.htm?source=govdelivery
Contact:
Consumers:
(563) 203-4671
FOR IMMEDIATE RELEASE - August 8, 2012 -Menno Beachy of Cresco, Iowa, is recalling one pint containers of Certified Organic Grape Tomatoes because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail, or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e. infected aneurysms), endocarditis, and arthritis.
A food distributor in Minnesota distributed 15 cases containing 12 one-pint containers of the affected grape tomatoes to retail stores located in Minnesota, Wisconsin, and Michigan between 7/26/12-8/6/12.
The grape tomatoes are packaged in square-shaped clear plastic clamshell containers labeled as Menno Beachy Certified Organic Grape Tomato, UPC number 044419310176, with a net weight of one pint. There are no lot numbers or expiration dates on the clamshell label. The clamshell packages are distributed in cases that are printed with a lot number. The case lot numbers affected by the recall are MB725GT3, MB725GT8, and MB725GT0.
No illnesses have been associated with the product.
Menno Beachy became aware of the contamination after the Minnesota Department of Agriculture collected a sample of the grape tomatoes located at the Minnesota distributor. The sample of lot number MB725GT0 found the grape tomatoes to be contaminated with Salmonella. Menno Beachy is investigating the source of the contamination.
Consumers who have the affected product should either discard it in the trash or return it to the point of purchase. Consumers with questions can leave a message on Menno Beachy’s voice mailbox at 563-203-4671 and he will return your call.
Cilantro salmonella warning for MN, WI
August 10, 2012
http://minnesota.publicradio.org/display/web/2012/08/10/health/cilantro-salmonella-warning/
ST. PAUL, Minn. (AP) -- The Minnesota Department of Agriculture says consumers should not eat fresh cilantro sold at certain stores because of possible salmonella contamination.
Routine testing found a sample of the product contaminated with salmonella.
The fresh cilantro was sold in bunches that were shipped to retailers in Minnesota, Wisconsin and Michigan between July 26 and Aug. 6. All stores that received the cilantro have been notified to remove the product from their shelves.
The advisory applies only to cilantro shipped to the stores between July 26 and Aug. 6.
Consumers who bought the cilantro bunches are advised to throw them out or return them to the store for a refund.
No illnesses have been reported.
Minnesota is working with California regulators to determine the source of the product.
Menno Beachy Recalls Grape Tomatoes Because Of Possible Health Risk
Limited Distribution In Minnesota, Wisconsin, And Michiganhttp://www.fda.gov/Safety/Recalls/ucm314871.htm?source=govdelivery
Contact:
Consumers:
(563) 203-4671
FOR IMMEDIATE RELEASE - August 8, 2012 -Menno Beachy of Cresco, Iowa, is recalling one pint containers of Certified Organic Grape Tomatoes because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail, or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e. infected aneurysms), endocarditis, and arthritis.
A food distributor in Minnesota distributed 15 cases containing 12 one-pint containers of the affected grape tomatoes to retail stores located in Minnesota, Wisconsin, and Michigan between 7/26/12-8/6/12.
The grape tomatoes are packaged in square-shaped clear plastic clamshell containers labeled as Menno Beachy Certified Organic Grape Tomato, UPC number 044419310176, with a net weight of one pint. There are no lot numbers or expiration dates on the clamshell label. The clamshell packages are distributed in cases that are printed with a lot number. The case lot numbers affected by the recall are MB725GT3, MB725GT8, and MB725GT0.
No illnesses have been associated with the product.
Menno Beachy became aware of the contamination after the Minnesota Department of Agriculture collected a sample of the grape tomatoes located at the Minnesota distributor. The sample of lot number MB725GT0 found the grape tomatoes to be contaminated with Salmonella. Menno Beachy is investigating the source of the contamination.
Consumers who have the affected product should either discard it in the trash or return it to the point of purchase. Consumers with questions can leave a message on Menno Beachy’s voice mailbox at 563-203-4671 and he will return your call.
Cilantro salmonella warning for MN, WI
August 10, 2012
http://minnesota.publicradio.org/display/web/2012/08/10/health/cilantro-salmonella-warning/
ST. PAUL, Minn. (AP) -- The Minnesota Department of Agriculture says consumers should not eat fresh cilantro sold at certain stores because of possible salmonella contamination.
Routine testing found a sample of the product contaminated with salmonella.
The fresh cilantro was sold in bunches that were shipped to retailers in Minnesota, Wisconsin and Michigan between July 26 and Aug. 6. All stores that received the cilantro have been notified to remove the product from their shelves.
The advisory applies only to cilantro shipped to the stores between July 26 and Aug. 6.
Consumers who bought the cilantro bunches are advised to throw them out or return them to the store for a refund.
No illnesses have been reported.
Minnesota is working with California regulators to determine the source of the product.
Monday, August 6, 2012
RTE Meals Recalled Due to Potential Presence of Listeria monocytogenes
Reichel Foods of Rochester, Minn is recalling 15880 pounds of ready-to-eat meals, called Armour Active Packs, due to the potential presence of Listeria monocytogenes. The contamination issue was discovered through 3rd party testing. There have been no reported illnesses. Product was shipped to 4 states (PA, TX, IN, and MN.)
The product is a multi-unit product targeted for children. Within the pack, there is a meat and cheese wrap long with an apple and apple dip. Since children are considered a high risk group, it is especially concerning.
Listeria monocytogenes contamination would most likely come from the plant environment. In a product like this, we may see the opportunity for contamination coming from the slicing of meat (or shredding of cheese), layering of meat and cheese onto the bread, and/or the packing of the wrap into the case.
Plants packing product like this would be expected to have a stout Listeria control plan in place, which would include sanitation, hygienic control during processing, and an environmental monitoring program.
USDA New Release
http://www.fsis.usda.gov/News_&_Events/Recall_053_2012_Release/index.asp
Minnesota Firm Recalls Ready-To-Eat Meat and Poultry Products Due To Potential Listeria Monocytogenes Contamination
Recall Release CLASS I RECALL
FSIS-RC-053-2012 HEALTH RISK: HIGH
Congressional and Public Affairs
Bill Bagley
(202) 720-0286
WASHINGTON, August 5, 2012 – Reichel Foods, a Rochester, Minn. establishment, is recalling approximately 15,880 pounds of ready-to-eat meat and poultry products due to possible contamination with Listeria monocytogenes, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.
The products subject to recall include: [View Labels (PDF Only)]
5.6 oz. packages of "Armour Active Packs Turkey & Cheese Wrap" Package Code 1026090112 or Case Code 27815-17994
5.6 oz. packages of "Armour Active Packs Ham & Cheese Wrap" Package Code 1026090112 or Case Code 27815-17995
All the products were produced between July 23, 2012, and July 26, 2012, and have a "sell by" date of Sept. 1, 2012. The packages bear the establishment number "P-19941" or "Est. 19941" inside the USDA mark of inspection. The products were shipped to distribution centers in Indiana, Minnesota, Pennsylvania, and Texas. When available, the retail distribution list will be posted on FSIS' website at www.fsis.usda.gov/
FSIS_Recalls/
Open_Federal_Cases/
index.asp.
The problem was discovered by the establishment, through microbiological testing by a third party. FSIS and the company have not received reports of illnesses due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
The product is a multi-unit product targeted for children. Within the pack, there is a meat and cheese wrap long with an apple and apple dip. Since children are considered a high risk group, it is especially concerning.
Listeria monocytogenes contamination would most likely come from the plant environment. In a product like this, we may see the opportunity for contamination coming from the slicing of meat (or shredding of cheese), layering of meat and cheese onto the bread, and/or the packing of the wrap into the case.
Plants packing product like this would be expected to have a stout Listeria control plan in place, which would include sanitation, hygienic control during processing, and an environmental monitoring program.
USDA New Release
http://www.fsis.usda.gov/News_&_Events/Recall_053_2012_Release/index.asp
Minnesota Firm Recalls Ready-To-Eat Meat and Poultry Products Due To Potential Listeria Monocytogenes Contamination
Recall Release CLASS I RECALL
FSIS-RC-053-2012 HEALTH RISK: HIGH
Congressional and Public Affairs
Bill Bagley
(202) 720-0286
WASHINGTON, August 5, 2012 – Reichel Foods, a Rochester, Minn. establishment, is recalling approximately 15,880 pounds of ready-to-eat meat and poultry products due to possible contamination with Listeria monocytogenes, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today.
The products subject to recall include: [View Labels (PDF Only)]
5.6 oz. packages of "Armour Active Packs Turkey & Cheese Wrap" Package Code 1026090112 or Case Code 27815-17994
5.6 oz. packages of "Armour Active Packs Ham & Cheese Wrap" Package Code 1026090112 or Case Code 27815-17995
All the products were produced between July 23, 2012, and July 26, 2012, and have a "sell by" date of Sept. 1, 2012. The packages bear the establishment number "P-19941" or "Est. 19941" inside the USDA mark of inspection. The products were shipped to distribution centers in Indiana, Minnesota, Pennsylvania, and Texas. When available, the retail distribution list will be posted on FSIS' website at www.fsis.usda.gov/
FSIS_Recalls/
Open_Federal_Cases/
index.asp.
The problem was discovered by the establishment, through microbiological testing by a third party. FSIS and the company have not received reports of illnesses due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
Sunday, August 5, 2012
NC Company Recalls Cantaloupes Due to Listeria
Burch Equipment of North Carolina is recalling approximate 189,000 cantaloupes after a product tested positive for Listeria and a then follow-up inspection indicated sanitary issues at the packing facility. There have been no reported illnesses. Product has been shipped to over 10 different states.
Interesting was that the tests were preformed by the USDA Microbiological Data Program, a program that was on the government chopping block just a few weeks ago. One may figure that this would help their future survival, and be a warning to other produce packers that a program fighting for survival may be working a bit harder to find contaminated product and nab few big headlines.
One would have figured that after the Jenson Cantaloupe Listeria issue, anyone packing cantaloupe would have paid close attention to the issues and then went to some great extremes to put in Listeria control measures in place. But clearly there are some who are not reading the paper and seeing the implications..implications not only for the company, but for the lareger industry. And really, this needs to extend to those packing any type of produce item that has the potential to support Listeria.
FDA Recall -- Firm Press Release
http://www.fda.gov/Safety/Recalls/ucm314213.htm
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Burch Equipment LLC Corrects Cantaloupe Variety Subject to Recall
Contact:
Consumer:
910-267-5781burch@intrstar.net
FOR IMMEDIATE RELEASE - August 3, 2012 - Burch Equipment LLC, North Carolina, is correcting the variety of cantaloupe involved in recalls initiated on July 28 and August 2, 2012. Previous announcements incorrectly identified the cantaloupes as being the Athena variety. The cantaloupes affected by the recall are the Caribbean Gold variety.
Athena cantaloupes are not subject to the recall.
Today’s announcement is not an expansion of the recall; no additional products are being recalled at this time.
The firm voluntarily recalled 580 cases of cantaloupes on July 28, and voluntarily recalled an additional 13,888 cases of cantaloupes (9 cantaloupes per case) and 581 bins of cantaloupes (110 cantaloupes per bin) on August 2, due to the potential for being contaminated with Listeria monocytogenes. Melons affected by this recall total 188,902.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The whole Caribbean Gold variety cantaloupes were shipped between July 15th and July 27th and distributed in FL, GA, IL, MD, ME, NC, NJ, NY, PA, SC and VA. The whole cantaloupes are identified by a red label reading Burch Farms referencing PLU # 4319. All cantaloupes involved in the recall were grown by Burch Farms, however some of the cantaloupes may have been identified with a "Cottle Strawberry, Inc." sticker referencing PLU #4319. Cottle Farms is not involved in this recall. Cantaloupes from Burch Farms were shipped in both corrugated boxes (9 cantaloupe per case) and in bulk bins.
Burch Equipment LLC is requesting any consumer that may have one of these cantaloupes to discard the product.
There have been no illnesses reported to date. FDA and the North Carolina Department of Agriculture and Consumer Services are working with Burch Equipment LLC following a random sample of a Caribbean Gold variety cantaloupe testing positive for Listeria monocytogenes. The recall expansion was based on unsanitary conditions found at the cantaloupe packing shed during FDA’s ongoing inspection that may allow for contamination of cantaloupes with Listeria monocytogenes.
Questions can be directed to Burch Equipment LLC at 910-267-5781 Monday through Friday, (9:00am to 4:00pm) or email burch@intrstar.net
FDA finds unsanitary conditions at Burch Farms packing shed
The Packer 08/02/2012 4:55:00 PM
Coral Beach http://www.thepacker.com/fruit-vegetable-enewsletter/Week_In_Review/164806206.html
A recall of about 5,200 Athena cantaloupes in two states ballooned to more than 188,900 cantaloupes distributed in 10 states after inspectors found “unsanitary conditions” at Burch Equipment LLC’s cantaloupe packing facility.
The Faison, N.C., grower, which operates under the name Burch Farms, initially recalled 580 cases of cantaloupes July 28. A positive result for listeria from a random sampling by the U.S. Department of Agriculture’s Microbiological Data Program sparked the recall.
The voluntary recall expanded Aug. 2 to include 13,888 cases and 581 bulk bins of the Athena melons. No illnesses had been reported, according to the Aug. 2 recall notice. The cases each hold nine melons and the bins each have 110 cantaloupes.
“The recall expansion is based on unsanitary conditions found at the cantaloupe packing shed during FDA’s ongoing inspection that may allow for contamination of cantaloupes with listeria monocytogenes,” the Aug. 2 notice states.
Interesting was that the tests were preformed by the USDA Microbiological Data Program, a program that was on the government chopping block just a few weeks ago. One may figure that this would help their future survival, and be a warning to other produce packers that a program fighting for survival may be working a bit harder to find contaminated product and nab few big headlines.
One would have figured that after the Jenson Cantaloupe Listeria issue, anyone packing cantaloupe would have paid close attention to the issues and then went to some great extremes to put in Listeria control measures in place. But clearly there are some who are not reading the paper and seeing the implications..implications not only for the company, but for the lareger industry. And really, this needs to extend to those packing any type of produce item that has the potential to support Listeria.
FDA Recall -- Firm Press Release
http://www.fda.gov/Safety/Recalls/ucm314213.htm
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Burch Equipment LLC Corrects Cantaloupe Variety Subject to Recall
Contact:
Consumer:
910-267-5781burch@intrstar.net
FOR IMMEDIATE RELEASE - August 3, 2012 - Burch Equipment LLC, North Carolina, is correcting the variety of cantaloupe involved in recalls initiated on July 28 and August 2, 2012. Previous announcements incorrectly identified the cantaloupes as being the Athena variety. The cantaloupes affected by the recall are the Caribbean Gold variety.
Athena cantaloupes are not subject to the recall.
Today’s announcement is not an expansion of the recall; no additional products are being recalled at this time.
The firm voluntarily recalled 580 cases of cantaloupes on July 28, and voluntarily recalled an additional 13,888 cases of cantaloupes (9 cantaloupes per case) and 581 bins of cantaloupes (110 cantaloupes per bin) on August 2, due to the potential for being contaminated with Listeria monocytogenes. Melons affected by this recall total 188,902.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The whole Caribbean Gold variety cantaloupes were shipped between July 15th and July 27th and distributed in FL, GA, IL, MD, ME, NC, NJ, NY, PA, SC and VA. The whole cantaloupes are identified by a red label reading Burch Farms referencing PLU # 4319. All cantaloupes involved in the recall were grown by Burch Farms, however some of the cantaloupes may have been identified with a "Cottle Strawberry, Inc." sticker referencing PLU #4319. Cottle Farms is not involved in this recall. Cantaloupes from Burch Farms were shipped in both corrugated boxes (9 cantaloupe per case) and in bulk bins.
Burch Equipment LLC is requesting any consumer that may have one of these cantaloupes to discard the product.
There have been no illnesses reported to date. FDA and the North Carolina Department of Agriculture and Consumer Services are working with Burch Equipment LLC following a random sample of a Caribbean Gold variety cantaloupe testing positive for Listeria monocytogenes. The recall expansion was based on unsanitary conditions found at the cantaloupe packing shed during FDA’s ongoing inspection that may allow for contamination of cantaloupes with Listeria monocytogenes.
Questions can be directed to Burch Equipment LLC at 910-267-5781 Monday through Friday, (9:00am to 4:00pm) or email burch@intrstar.net
FDA finds unsanitary conditions at Burch Farms packing shed
The Packer 08/02/2012 4:55:00 PM
Coral Beach http://www.thepacker.com/fruit-vegetable-enewsletter/Week_In_Review/164806206.html
A recall of about 5,200 Athena cantaloupes in two states ballooned to more than 188,900 cantaloupes distributed in 10 states after inspectors found “unsanitary conditions” at Burch Equipment LLC’s cantaloupe packing facility.
The Faison, N.C., grower, which operates under the name Burch Farms, initially recalled 580 cases of cantaloupes July 28. A positive result for listeria from a random sampling by the U.S. Department of Agriculture’s Microbiological Data Program sparked the recall.
The voluntary recall expanded Aug. 2 to include 13,888 cases and 581 bulk bins of the Athena melons. No illnesses had been reported, according to the Aug. 2 recall notice. The cases each hold nine melons and the bins each have 110 cantaloupes.
“The recall expansion is based on unsanitary conditions found at the cantaloupe packing shed during FDA’s ongoing inspection that may allow for contamination of cantaloupes with listeria monocytogenes,” the Aug. 2 notice states.
Friday, August 3, 2012
Onion Recall Cascades as Customers Recall Products Made with Suspect Onions
The Gill Onion recall is cascading as a number of retail chains are recalling products made with the recalled onions. To date, there have been a dozen or so companies recalling products made with the recalled onions. Here, like so many past recalls, we can see the impact of upstream suppliers on their customers. Traceability is key in that you know who your suppliers are, and where their product is being used.
The best news is that there have been no illnesses to date. In such a big recall, you might expect to have some illnesses associated with the product. So what are some reasons. Certainly luck may be a part of it, but there may be a few others that impact this:
- Low level of contamination.
- The Listeria monocytogenes serotype involved – As per Dr. Steve Knabel ‘of the 13 serotypes, there are 4 that account for the vast majority of cases of human illness.’ There are serotypes of L. monocytogenes that do not have the necessary genes to cause disease. While it is unknown at this point if this is the case, we can’t assume that it is. Further, if the conditions in the processing facility supported one serotype of L. monocytogenes, then it often assumed that those conditions can support the more virulent strains.
Gills recall sparks dozens of related product recalls
08/02/2012 3:06:26 PM
Coral Beachhttp://www.thepacker.com/fruit-vegetable-news/Gills-recall-sparks-dozens-of-product-recalls-164791766.html
A recall of one day’s production from a Gills Onions plant — that was expanded a week later to an “undeterminable” volume — caused a cascade effect as retailers and processors recalled more than 150 fresh products.
As of Aug. 2, fears of listeria contamination spurred five retail chains and seven fresh food producers to voluntarily recall products because they included recalled Gills onions.
No illnesses have been linked to any of the recalled produce or fresh products, according to multiple FDA recall notices at http://tinyurl.com/FDA-recalls.
Gills, Oxnard, Calif., initially recalled about 6,000 pounds of fresh-cut onions and celery July 18 after a random sample taken at retail by the Food and Drug Administration tested positive for listeria.
The company expanded the recall July 26 to include an unknown volume of whole onions and other chopped onions because investigators found listeria at one of Gills’ two Oxnard fresh-cut facilities. That facility has been closed since July 17 when FDA officials notified Gills of the positive test at retail, according to Gills spokeswoman Amy Philpott.
“Because the July 25 expanded recall does not include a beginning use-by-date, but rather included recalled products with use-by dates on or before Aug. 3, the number of recalled pounds is undeterminable,” according to a Gills onion statement.
“In the interest of public health, the company simply included all recalled products in the marketplace,” according to the release.
Philpott said the facility will remain closed until the listeria contamination problem is resolved. Gills continues to operate another processing facility in a separate building.
“They are running extra shifts, but orders are a bit behind,” Philpott said, adding that some retail and specialty product orders probably will not be met.
“Steve Gill has said it will take as long as it takes to resolve the problem.”
Gill has not been available for interviews, but he did include a statement in the recall notice: “We’ve identified the problem, and we are taking aggressive actions to prevent this from happening again.”
The actions include forming a panel of food safety experts and microbiologists with expertise in listeria control, expanding required microbial surveillance and sanitation programs, and continued testing.
“They also have a team looking at possibly redesigning the facility,” Philpott said.
In late May Gills recalled 2,360 pounds of diced red onions in the U.S. and Canada after the Canadian Food Inspection Agency did a random sample and got a positive result for listeria.
Gills built both of the facilities in Oxnard in the late 90s, Philpott said, and both were built specifically for onion processing. Gills started producing in the facility that is now shut down 15 years ago. The other facility, which is larger, opened 12 years ago.
As of the Aug 2, FDA’s recall Web page showed the following recalls related to the recalled Gills onions:
Simmering Soup Inc., Atlanta, recalled Trader Joe’s brand salsas and balela;
Whole Foods Markets recalled about 35 fresh food products in Florida stores;
Cool Creations LLC, North Kansas City, Mo., recalled about 20 fresh food products;
Wegmans Food Markets Inc. recalled six fresh food products;
GH Foods CA LLC recalled almost 90 fresh food products under a variety of store and specialty brands, including: Delish, Albertsons generic label, Garden Highway, Marketside, Natural Directions, Pacific Coast, Raley’s, Safeway Farms, Signature Cafe, Sprouts and Trader Joe’s;
Huxtable’s Kitchen, recalled Trader Joe’s brand roasted butternut squash, red quinoa and wheatberry salad;
Stop & Shop Supermarket Co. LLC recalled Costa Fruit & Produce brand calico bean salad from salad bars;
Spartan Stores, Grand Rapids, Mich., recalled Spartan Fresh Selections three bean salad and broccoli stir fry products;
Publix Super Markets recalled custom sub sandwiches that contain onions;
Ken’s Foods Inc. recalled cole slaw sauce, baked bean sauce and three brands of tartar sauce;
Garden Fresh Foods Inc. recalled ready-to-eat salads, slaw, salsa, bean and dip products; and
San Miguel Produce Inc., Oxnard, recalled packaged salad kits under the Cut ‘N Clean brand.
The best news is that there have been no illnesses to date. In such a big recall, you might expect to have some illnesses associated with the product. So what are some reasons. Certainly luck may be a part of it, but there may be a few others that impact this:
- Low level of contamination.
- The Listeria monocytogenes serotype involved – As per Dr. Steve Knabel ‘of the 13 serotypes, there are 4 that account for the vast majority of cases of human illness.’ There are serotypes of L. monocytogenes that do not have the necessary genes to cause disease. While it is unknown at this point if this is the case, we can’t assume that it is. Further, if the conditions in the processing facility supported one serotype of L. monocytogenes, then it often assumed that those conditions can support the more virulent strains.
Gills recall sparks dozens of related product recalls
08/02/2012 3:06:26 PM
Coral Beachhttp://www.thepacker.com/fruit-vegetable-news/Gills-recall-sparks-dozens-of-product-recalls-164791766.html
A recall of one day’s production from a Gills Onions plant — that was expanded a week later to an “undeterminable” volume — caused a cascade effect as retailers and processors recalled more than 150 fresh products.
As of Aug. 2, fears of listeria contamination spurred five retail chains and seven fresh food producers to voluntarily recall products because they included recalled Gills onions.
No illnesses have been linked to any of the recalled produce or fresh products, according to multiple FDA recall notices at http://tinyurl.com/FDA-recalls.
Gills, Oxnard, Calif., initially recalled about 6,000 pounds of fresh-cut onions and celery July 18 after a random sample taken at retail by the Food and Drug Administration tested positive for listeria.
The company expanded the recall July 26 to include an unknown volume of whole onions and other chopped onions because investigators found listeria at one of Gills’ two Oxnard fresh-cut facilities. That facility has been closed since July 17 when FDA officials notified Gills of the positive test at retail, according to Gills spokeswoman Amy Philpott.
“Because the July 25 expanded recall does not include a beginning use-by-date, but rather included recalled products with use-by dates on or before Aug. 3, the number of recalled pounds is undeterminable,” according to a Gills onion statement.
“In the interest of public health, the company simply included all recalled products in the marketplace,” according to the release.
Philpott said the facility will remain closed until the listeria contamination problem is resolved. Gills continues to operate another processing facility in a separate building.
“They are running extra shifts, but orders are a bit behind,” Philpott said, adding that some retail and specialty product orders probably will not be met.
“Steve Gill has said it will take as long as it takes to resolve the problem.”
Gill has not been available for interviews, but he did include a statement in the recall notice: “We’ve identified the problem, and we are taking aggressive actions to prevent this from happening again.”
The actions include forming a panel of food safety experts and microbiologists with expertise in listeria control, expanding required microbial surveillance and sanitation programs, and continued testing.
“They also have a team looking at possibly redesigning the facility,” Philpott said.
In late May Gills recalled 2,360 pounds of diced red onions in the U.S. and Canada after the Canadian Food Inspection Agency did a random sample and got a positive result for listeria.
Gills built both of the facilities in Oxnard in the late 90s, Philpott said, and both were built specifically for onion processing. Gills started producing in the facility that is now shut down 15 years ago. The other facility, which is larger, opened 12 years ago.
As of the Aug 2, FDA’s recall Web page showed the following recalls related to the recalled Gills onions:
Simmering Soup Inc., Atlanta, recalled Trader Joe’s brand salsas and balela;
Whole Foods Markets recalled about 35 fresh food products in Florida stores;
Cool Creations LLC, North Kansas City, Mo., recalled about 20 fresh food products;
Wegmans Food Markets Inc. recalled six fresh food products;
GH Foods CA LLC recalled almost 90 fresh food products under a variety of store and specialty brands, including: Delish, Albertsons generic label, Garden Highway, Marketside, Natural Directions, Pacific Coast, Raley’s, Safeway Farms, Signature Cafe, Sprouts and Trader Joe’s;
Huxtable’s Kitchen, recalled Trader Joe’s brand roasted butternut squash, red quinoa and wheatberry salad;
Stop & Shop Supermarket Co. LLC recalled Costa Fruit & Produce brand calico bean salad from salad bars;
Spartan Stores, Grand Rapids, Mich., recalled Spartan Fresh Selections three bean salad and broccoli stir fry products;
Publix Super Markets recalled custom sub sandwiches that contain onions;
Ken’s Foods Inc. recalled cole slaw sauce, baked bean sauce and three brands of tartar sauce;
Garden Fresh Foods Inc. recalled ready-to-eat salads, slaw, salsa, bean and dip products; and
San Miguel Produce Inc., Oxnard, recalled packaged salad kits under the Cut ‘N Clean brand.
Friday, July 27, 2012
Gill Onions expands recall of fresh cut onions and celery due to Listeria
Gill Onions of Oxnard CA is expanding its recall due to fact product may be contaminated with Listeria monocytogenes. According to the FDA release, the expanded product
list includes diced, slivered and whole peeled onions and diced onion/celery
mix with use-by-dates on or before August 3. http://www.fda.gov/Safety/Recalls/ucm313399.htm
This recall expands upon the initial recall that was issued on July 18th. http://pennstatefoodsafety.blogspot.com/2012/07/fresh-cut-onions-and-celery-recalled.html
How can this happen.? While the initial recall was based upon a product from retail testing positive, the expanded recall occurred when in-plant testing found more positive Listeria tests. (http://www.thepacker.com/fruit-vegetable-news/Gills-expands-onion-celery-recall-listeria-found-at-plant-163863626.html). Finding Listeria in the plant environment led officials to believe that the Listeria issue was not a single lot issue, but was wider spread within the facility and thus implicated product over multiple lots.
After the cantaloupe recall earlier this year, there has been increasing attention to RTE produce, primarily products like this that have been further processed in some way. Products like these onions which were sliced, can get contaminated during processing if that process and the environment has not been maintained to the level needed to control Listeria monocytogenes. In order to do this, processing facilities must have adequate controls including stout sanitation program but then must also verify that Listeria is not present through an environmental monitoring program.
As indicated in the Packer article, the facility may need to be redesigned. This is certainly an issue in older plants find that find they need to make changes in order to meet this increased standard of Listeria free.
This recall expands upon the initial recall that was issued on July 18th. http://pennstatefoodsafety.blogspot.com/2012/07/fresh-cut-onions-and-celery-recalled.html
How can this happen.? While the initial recall was based upon a product from retail testing positive, the expanded recall occurred when in-plant testing found more positive Listeria tests. (http://www.thepacker.com/fruit-vegetable-news/Gills-expands-onion-celery-recall-listeria-found-at-plant-163863626.html). Finding Listeria in the plant environment led officials to believe that the Listeria issue was not a single lot issue, but was wider spread within the facility and thus implicated product over multiple lots.
After the cantaloupe recall earlier this year, there has been increasing attention to RTE produce, primarily products like this that have been further processed in some way. Products like these onions which were sliced, can get contaminated during processing if that process and the environment has not been maintained to the level needed to control Listeria monocytogenes. In order to do this, processing facilities must have adequate controls including stout sanitation program but then must also verify that Listeria is not present through an environmental monitoring program.
As indicated in the Packer article, the facility may need to be redesigned. This is certainly an issue in older plants find that find they need to make changes in order to meet this increased standard of Listeria free.
Monday, July 23, 2012
Ground meat recalled after linked to salmonellosis cases
Upadate 8/6/12: CDC updated the number of illnesses to 40.
http://www.cdc.gov/salmonella/enteritidis-07-12/index.html
Cargill is recalling approximately 29339 lbs of ground beef after the product was linked to Salmonella enteritidis infections. The recalled product was produced on May 25, 2012 and although the product would be past the expiration date, there is concern that some may still have this meat in thier freezer.
The strain that was responsible for this illness, Salmonella enteritidis or SE, is more often associated with poultry. According to the CDC - "Eggs have been the most common food source linked to SE infections.....Since the early 2000s, poultry has also been found to be a common food source for SE infections. Multiple other, less frequently identified sources include raw milk, pork, beef, sprouts, and raw almonds."
Cargill sells chubs of meat to retailers who then repackage this product into retail sized packages. These packages will have the store brand on the label, but will show the same USDA establishment number 9400.
This is an interesting recall from the standpoint that this strain is not an antibiotic resistant strain of Salmonella and it was in raw meat, not a RTE product. Unlike E. coli STEC strains which are considered an adulterant in ground beef, Salmella is not. Cargill had recalled ground turkey for Salmonella, but those strains were antibiotic resistant and thus more difficult to treat. Well if we can expect that ground beef may have Salmonella present, then why recall? Since this strain in this product has been linked to at least 5 illnesses, USDA and Cargill decided it was in the best interest of the public. However, are we getting to a point when raw meat products will be expected to have no pathogens?
http://www.cdc.gov/salmonella/enteritidis-07-12/index.html
Cargill is recalling approximately 29339 lbs of ground beef after the product was linked to Salmonella enteritidis infections. The recalled product was produced on May 25, 2012 and although the product would be past the expiration date, there is concern that some may still have this meat in thier freezer.
The strain that was responsible for this illness, Salmonella enteritidis or SE, is more often associated with poultry. According to the CDC - "Eggs have been the most common food source linked to SE infections.....Since the early 2000s, poultry has also been found to be a common food source for SE infections. Multiple other, less frequently identified sources include raw milk, pork, beef, sprouts, and raw almonds."
Cargill sells chubs of meat to retailers who then repackage this product into retail sized packages. These packages will have the store brand on the label, but will show the same USDA establishment number 9400.
This is an interesting recall from the standpoint that this strain is not an antibiotic resistant strain of Salmonella and it was in raw meat, not a RTE product. Unlike E. coli STEC strains which are considered an adulterant in ground beef, Salmella is not. Cargill had recalled ground turkey for Salmonella, but those strains were antibiotic resistant and thus more difficult to treat. Well if we can expect that ground beef may have Salmonella present, then why recall? Since this strain in this product has been linked to at least 5 illnesses, USDA and Cargill decided it was in the best interest of the public. However, are we getting to a point when raw meat products will be expected to have no pathogens?
Friday, July 20, 2012
2nd recall for processor of RTE meat products due to Listeria
Buona Vita, a NJ meat processor, is issuing its 2nd recall this month for Listeria. In the last recall, products from a number of production dates in May were recalled. In this recall, products made on June 26th were recalled. According to the FSIS Release (below), the product was tested by a third party and found to be positive.
(Earlier recall http://pennstatefoodsafety.blogspot.com/2012/07/nj-firm-recalling-frozen-meat-product.html)
Bridgeton meat company issues second voluntary recall in July
Published: Thursday, July 19, 2012, 8:25 PM Updated: Thursday, July 19, 2012, 8:48 PM
By Jason Laday/The News of Cumberland County
http://www.nj.com/cumberland/index.ssf/2012/07/bridgeton_meat_company_issues.html
BRIDGETON — Buona Vita, Inc. is recalling an additional 72,510 pounds of frozen meat and poultry products due to possible Listeria monocytogenes contamination.
In an announcement released Thursday evening, officials from the United States Department of Agriculture (USDA) Food Safety and Inspection Service (FSIS) stated 15 more products made by the Bridgeton-based meat company are being voluntarily recalled, and pose a “high” health risk.
(Earlier recall http://pennstatefoodsafety.blogspot.com/2012/07/nj-firm-recalling-frozen-meat-product.html)
Bridgeton meat company issues second voluntary recall in July
Published: Thursday, July 19, 2012, 8:25 PM Updated: Thursday, July 19, 2012, 8:48 PM
By Jason Laday/The News of Cumberland County
http://www.nj.com/cumberland/index.ssf/2012/07/bridgeton_meat_company_issues.html
BRIDGETON — Buona Vita, Inc. is recalling an additional 72,510 pounds of frozen meat and poultry products due to possible Listeria monocytogenes contamination.
In an announcement released Thursday evening, officials from the United States Department of Agriculture (USDA) Food Safety and Inspection Service (FSIS) stated 15 more products made by the Bridgeton-based meat company are being voluntarily recalled, and pose a “high” health risk.
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