Nestle recalls Nesquick Chocolate Powder

Nestle is recalling Nesquick Chocolate Powder after the supplier of one the product’s ingredient issued a recall.  The ingredient, calcium carbonate, was being recalled due to the possible presence of Salmonella.  There have been no reports of illness.

 

Nestlé USA Announces Voluntary Recall of NESQUIK® Chocolate Powder

http://www.fda.gov/Safety/Recalls/ucm327533.htm

FOR IMMEDIATE RELEASE - November 8, 2012 - Nestlé USA announced the voluntary recall of limited quantities of Nestlé NESQUIK® Chocolate Powder in the 10.9, 21.8 and 40.7 ounce canisters. The voluntary recall is limited to only NESQUIK Chocolate Powder, which was distributed nationally. No other varieties of NESQUIK powder or any sizes or flavors of NESQUIK ready-to-drink are affected by this recall.

Nestlé is removing the canisters from distribution because the company was notified by an ingredient supplier, Omya Inc. that it has issued a recall of certain lots of its ingredient, calcium carbonate due to possible presence of Salmonella. Calcium carbonate is used in NESQUIK as an ingredient. There have been no reports of any illnesses or adverse health effects associated with the affected product.

To ensure the safety of consumers, Nestlé is recalling selected NESQUIK Chocolate Powder. The recall is limited to the following sizes, UPC and production codes of NESQUIK Chocolate Powder:

Size	UPC Code	Production Codes
40.7 oz. Chocolate (72 servings)	0 28000 68230 9	2282574810 2282574820
21.8 oz. Chocolate (38 servings)	0 28000 68090 9	2278574810 2278574820 2279574810 2279574820 2284574820 2284574830 2285574810 2285574820 2287574820 2289574810 2289574820
10.9 oz. Chocolate (19 servings)	0 28000 67990 3	2278574810

The affected NESQUIK Chocolate Powder was produced during early October, 2012. To locate the production code, consumers should look on the bottom of the canister, adjacent to the consumer expiration date. All affected products have an expiration date of BEST BEFORE Oct 2014.

Consumers who may have purchased the affected NESQUIK Chocolate Powder should not consume it, but instead should return it to the place of purchase for a full refund or contact Nestlé Consumer Services at (800) 628-7679.

The most common symptoms of Salmonella infection are diarrhea, abdominal cramps and fever, which develop within eight to 72 hours of eating or drinking contaminated food. The illness usually lasts for four to seven days and most people recover without treatment. However, salmonellosis can be severe or even life threatening for infants, older people, pregnant women and those with weakened immune systems. Individuals experiencing these symptoms should seek medical attention.

Nestlé is dedicated to the health and safety of its consumers. For these reasons, the company initiated this voluntary recall. We apologize to our consumers and sincerely regret any inconvenience created by this incident.

Wegmans spinanch salad mix and Bolthouse sliced carrots recalled

There are two produce related recalls.

 - Wegman’s is recalling it Organic Spinach and Spring Mix Blend after it was linked to now 19 cases of E. coli O157:H7 cases in New York. The product was co-packed for Wegman’s by Massachusetts based Spring Garden. The product was sold between Oct 14th and Nov 1st.

 - Bolthouse Foods of Bakersfield CA is recalling carrot chips. A sample of the carrot chips were tested by NC Health and found to be positive for Salmonella. There have been no reported illnesses. Product was co-packed for store brands including Safeway Farms and Supervalu’s Farm Stand.


Three more E. coli cases added to outbreak
Wegmans recalled spinach and spring mixes due to outbreak

Democrat and Chronicle.com 10:05 PM, Nov 5, 2012http://www.democratandchronicle.com/article/20121105/NEWS01/311050058

Three additional cases of E. coli have been linked to organic spinach and spring mix blends sold by Wegmans Food Markets.

Guideance for Food Operations Exposed to Floods and Hurricanes

When a major disaster strikes, the safety of food becomes a major question.  In some cases refrigeration is lost for several days, in other cases, food is exposed to contaminated water.

For consumers, careful evaluation is needed for those foods stored in a the refrigerator or freezer that has lost electrical power ( http://extension.psu.edu/food-safety/news/2012/power-outages-and-freezer-failures , http://www.fda.gov/Food/ResourcesForYou/Consumers/ucm076881.htm) and what to do when returning to a home that has been in a hurricane or flood (http://www.fda.gov/Food/ResourcesForYou/Consumers/ucm076993.htm).

For businesses that handle food, FDA provides guidance for disasters.

·        Handling of food items exposed to flood waters (http://www.fda.gov/Food/FoodDefense/Emergencies/FloodsHurricanesPowerOutages/ucm112723.htm).  It is important to note that jars with screw tops and bottles with crimp lids (beer and soda bottles) be destroyed.  The reason for this is that debris may become lodged in the space between the cap and jar.   

·        Disposal of food items (http://www.fda.gov/Food/FoodDefense/Emergencies/FloodsHurricanesPowerOutages/ucm112717.htm)

·        Restaurants and Grocers reopening after flood or hurricane (http://www.fda.gov/Food/FoodDefense/Emergencies/FloodsHurricanesPowerOutages/ucm112713.htm)

·        Decontamination of transport vehicles (http://www.fda.gov/Food/FoodDefense/Emergencies/FloodsHurricanesPowerOutages/ucm112728.htm).

·        Water subject to a boil advisory (http://www.fda.gov/Food/GuidanceComplianceRegulatoryInformation/GuidanceDocuments/FoodDefenseandEmergencyResponse/ucm211373.htm).

·        Crops (http://www.fda.gov/Food/GuidanceComplianceRegulatoryInformation/GuidanceDocuments/FoodDefenseandEmergencyResponse/ucm274683.htm).

Problems at NECC facility that led to meningitis outbreak

This is not food related, but the issues seen at this facility that made the contaminated epidurals that led to the fungal meningitis outbreak provide lessons in product and environmental control.

 · Firm shipped product before receiving sterility results (results were negative however).

· Firm didn't follow established standards for autoclaving and didn't keep products in the autoclave for the minimum 20 minutes needed to ensure sterility

· Firm didn't thoroughly clean powder hoods used to protect pharmacists while they prepare compounded substances. Investigators observed residual powder within the hood, which could lead to contamination of medications
· Mats designed to trap dirt and other contaminants were visibly soiled, and a leaking boiler next to the clean room caused water to pool around it and adjacent walls, creating conditions that could support contaminant growth, according to the findings.

In the report below, Massachusetts Governor Patrick states that over the years, some pharmacies have evolved from neighborhood drug stores to large-scale manufacturers that sell products across state lines, and that regulations in Massachusetts and at the federal level have not kept pace with the changes. He said that he had directed the pharmacy board to start making unannounced inspections of compounding pharmacies that make sterile injectable medications and strengthen penalties for pharmacies that don't comply with rules.

Not sure I want my local pharmacy making medicine, especially ones that can be injected in me. Dispensing medicine is one thing, but making it, no thanks.  

We see this type of thing in food companies as well…the firm expands into a niche outside of their core competency and grow the business, but never become technically competent in that new business. They fail to spend the capital on the facility needed to meet the requirements of producing that product. Then, as more product is shipped, the inevitable production error occurs, impacting far too many.


Report airs problems at firm linked to fungal meningitis outbreak
Lisa Schnirring Staff Writer
http://www.cidrap.umn.edu/cidrap/content/other/news/oct2412fungal2-jw.html

Oct 24, 2012 (CIDRAP News) – Massachusetts officials yesterday said New England Compounding Center (NECC), the firm linked to a multistate fungal meningitis outbreak, sent shipments from two of the recalled lots before it received sterility testing results. 

Investigators also found black particulate matter in several unopened vials of the recalled methylprednisolone acetate, which was used in epidural injections for back pain and injections for peripheral joint problems, according to a report of preliminary investigation findings.

Federal officials have said that as many as 14,000 patients could have been exposed to the recalled injections.

Nine more infections have been reported in the outbreak, raising the number of infections to 317, the US Centers for Disease Control and Prevention (CDC) said today in its latest update. One more death was reported, putting that total at 24, and the number of affected states held steady at 17. 

The CDC reported one more joint infection linked to the contaminated steroids, raising that number to five, and it said 54 cases have now been confirmed with lab tests. So far all but two of the infections involve Exserohilum rostratum, a type of black mold that hadn't previously been known to cause meningitis. 

In a press conference with reporters yesterday, Madeleine Biondolillo, MD, who directs the Massachusetts Department of Public Health's Bureau of Health Care Safety and Quality, said the investigation began on Sep 25 and involves collaboration with their colleagues at the US Food and Drug Administration (FDA) since Oct 1. She said the investigation is ongoing and that authorities have obtained evidence, reviewed NECC's standard operating procedures, probed the company's records, and interviewed its employees.

NECC didn't label the medications for specific patients, a violation of Massachusetts licensing regulations for compounding pharmacies, Biondolillo said.

According to the Massachusetts Department of Public Health (MDPH) investigation report, NECC's sterility tests on the shipments sent before results came in didn't show contamination. However, investigators said they were still exploring the adequacy of NECC's testing methods.

In addition, authorities found that the company didn't follow established standards for autoclaving and didn't keep products in the autoclave for the minimum 20 minutes needed to ensure sterility.

The report also says NECC didn't thoroughly clean powder hoods used to protect pharmacists while they prepare compounded substances. Investigators observed residual powder within the hood, which could lead to contamination of medications.

Mats designed to trap dirt and other contaminants were visibly soiled, and a leaking boiler next to the clean room caused water to pool around it and adjacent walls, creating conditions that could support contaminant growth, according to the findings.

At the media briefing, Massachusetts governor Deval Patrick said federal officials have launched a criminal investigation into NECC's actions and he announced more steps the state and its Board of Pharmacy have taken in response to the steroid contamination, including permanently revoking NECC's operating license and those of its three principal pharmacists.

"Those whose laboratory practices caused this outbreak should never practice pharmacy or manufacture in Massachusetts again," he said.

Patrick said that, over the years, some pharmacies have evolved from neighborhood drug stores to large-scale manufacturers that sell products across state lines, and that regulations in Massachusetts and at the federal level have not kept pace with the changes. He said that he had directed the pharmacy board to start making unannounced inspections of compounding pharmacies that make sterile injectable medications and strengthen penalties for pharmacies that don't comply with rules.

The state will now require compounding pharmacies in Massachusetts to submit annual production, volume, and distribution reports to make it easier for authorities to flag operations that are acting more like manufacturers, which require federal licensing and extra scrutiny, Patrick said. He added that the state will require compounding pharmacies to report interactions with federal regulators and will form a special commission to examine best practices in other states and what changes may be needed at the federal level.

Summary of the FDA Requirements for Food Facility Registration

The FDA has updated the registration process for food facilities and that registration is now open. According to the FDA, “Biennial Registration Renewal for Food Facilities began at 12:01 AM on October 22, 2012. The updated food facility registration system is accepting food facility registration renewals.” The registration, initially required under the Bioterrorism Act of 2002 was updated as part of the Food Safety Modernization Act of 2011.  

· It is required for any facilities, domestic or foreign that manufacture, process, pack, or hold food for human or animal consumption in the US, including those companies who produce products that do not enter interstate commerce.

· If you registered before, you must re-register

· Facilities must register from Oct 1 to Dec 31 of even numbered years (2012, 2014, etc) 

· Who does not need to register? Farms (that do not process), retail food establishments, restaurants, and non-profit that complies with 21 CFR 1.227(b) (7) and facilities that are regulated exclusively, throughout the entire facility, by the U.S. Department of Agriculture under the Federal Meat Inspection Act the Poultry Products Inspection Act or the Egg Products Inspection Act.);

· Email address for facility contacts now must be included.

· Registration information http://www.fda.gov/Food/FoodSafety/FSMA/ucm314178.htm


Food Facility Registration Requirements under the FDA Food Safety Modernization Act
http://www.fda.gov/Food/NewsEvents/ConstituentUpdates/ucm324801.htm
October 19, 2012

The U.S. Food and Drug Administration (FDA) today issued further information and guidance regarding registration requirements for domestic and foreign manufacturers, processors, packers or holders of food for human or animal consumption based on changes made by the FDA Food Safety Modernization Act (FSMA) to the Federal Food, Drug, and Cosmetic Act (FD&C Act). The updated food facility registration system will become available at 12:01 a.m. Monday morning, October 22, 2012.

Food producers and manufactures have long been required to register with the Food and Drug Administration. There is no fee to register or renew the registration of a food facility. Facilities can register online, via mail or fax. FDA encourages online registration as a quick and efficient means for food facility registration.

The Food Safety Modernization Act improves the registration process by ensuring, among other things, that the FDA has accurate contact information for each facility. The new registration form also includes new categories of foods. These new categories will help FDA rapidly communicate with the right facilities in the event of an emergency.  

Biennial registration renewal will become available at 12:01 a.m. Monday morning, October 22, 2012. To submit a registration renewal to FDA, a food facility is required to submit required registration information to FDA, including the additional registration information described above. To facilitate this process, the agency is offering technical assistance online and through the help desk. Please check FDA’s food facility registration website for more information and to register online.

Sunland Peanut Butter Recall Impacts Uncrustables

The Sunland Peanut Butter recall continues to drag on. The latest product recalled due to the use of the Sunland Peanut Butter – Smucker’s Uncrustables. Smucker’s points out that the recall only impacts the Uncrustables that were sold for USDA School Lunch Program, and not their other peanut butter related products. In fact, the Sunland product was only used for limited production runs of the Uncrustables. It is also important to not that there have been no illnesses linked to the Smucker’s product.

Companies often supplement their own supply with ingredients produced by others. When this occurs, especially with ingredients to be used in ready-to-eat applications, that purchaser has to make sure that the supplier has a stout food safety program. Companies spend countless millions of dollars establishing a well-respected brand, and can see it tarnished quickly by a less-than-stellar supplier.  

Smucker's Uncrustables sold to schools recalled

http://www.usatoday.com/story/news/nation/2012/10/19/smuckers-uncrustables-recall/1644249/

The J.M. Smucker Co. used peanut butter that was produced by Sunland, a company recently linked to salmonella illnesses.
12:44PM EDT October 19. 2012 - USAToday

 MINNEAPOLIS (AP) — Officials have told school lunch programs across the country to check to see whether they have any Smucker's Uncrustables sandwiches that might contain peanut butter made by a New Mexico company that is being recalled because of potential salmonella contamination.

The J.M. Smucker Co. used peanut butter that was produced by Sunland Inc. and supplied by the U.S. Department of Agriculture in "limited production runs" of 72-count bulk packs of the sandwiches that went to schools under the National School Lunch Program, Smucker's spokeswoman Maribeth Badertscher said in an e-mail Thursday.
Uncrustables are pre-made peanut butter and jelly, pocket-like, circular sandwiches.

 The Orrville, Ohio-based company tests all the incoming USDA-supplied peanut butter it gets, and tests finished products before distributing them, and found no problems, she said.

 But out of "an abundance of caution," and working with federal agencies, she said, Smucker's recently notified school customers that they should check to see if they still have any of the crustless frozen peanut butter and jelly sandwiches from the recalled lots, which all have either expired or will expire soon. They should not be served to students, the company said.

 No other Smucker's products contain peanut butter from Sunland or other outside suppliers, Badertscher said. She said she did not immediately know how many sandwiches were involved.

Sunland shut down its plant in Portales, N.M., last month and recalled more than 200 products made under a variety of brand names after salmonella was found in Trader Joe's Creamy Salted Valencia Peanut Butter. Thirty-five illnesses in 19 states have been linked to Sunland, but no illnesses have been linked to the Uncrustable sandwiches.

"When USDA learned of the FDA recall of certain products manufactured by Sunland, Inc., we coordinated with state agencies to immediately notify individual school districts and ensure that recalled products were identified and destroyed," USDA spokeswoman Alyn Kiel said in an e-mail.

The Smucker's recall was first reported by Food Poisoning Bulletin, a website published by Minneapolis-based food safety lawyer Fred Pritzker.

Copyright 2012 The Associated Press. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.

Fresh Express Recalls Bagged Lettuce Due to Potential Salmonella Contamination

Fresh Express, one of the leading manufacturers of ready-to-eat salads is recalling Romaine lettuce hearts.  Product tested as part of the FDA's random testing program was found to be positive for Salmonella.  No illnesses have been reported.

Fresh Express Issues Recall of Limited Quantity of 18 oz. Hearts of Romaine Salad Due to Possible Health Risk

http://www.fda.gov/Safety/Recalls/ucm323535.htm

FOR IMMEDIATE RELEASE - October 11, 2012 - Charlotte, North Carolina – Fresh Express Incorporated is conducting a voluntary, precautionary recall of a limited quantity of Fresh Express Hearts of Romaine Salad with a Use-by Date of October 11 and Product Code of S270A24 due to a possible health risk from Salmonella.

No illnesses or consumer complaints have been reported to Fresh Express at this time in association with this recall. No other Fresh Express products are subject to this recall.

The recall notification is being issued out of an abundance of caution based on an isolated instance in which a random sample yielded a positive result for Salmonella as part of the U.S. Food and Drug Administration’s random sample testing program. Fresh Express is coordinating closely with regulatory officials.

Fresh Express customer service representatives are already contacting relevant retailers to confirm the recalled product has been removed from store shelves and inventories and that none is available for consumer purchase. Customers with questions are instructed to contact their Fresh Express customer service representative. The recalled salads were distributed primarily in the West-Northwest and Midwest regions of the U.S.

Consumers who may have purchased the recalled salad are asked not to eat it, but to throw it out instead. Fresh Express is offering a full refund. Consumers with questions or who would like to secure a refund may call the Fresh Express Consumer Response Center at (800) 242-5472 during the hours of 8 a.m. to 7 p.m. Eastern Daylight Time.
Specific recall information follows:

 Product Being Recalled: Fresh Express Hearts of Romaine in 18 oz. package
Product Code: S270A24 (located in upper right corner on front of package)
Use-by Date: October 11 (also located in upper right hand corner of package)
Distribution: Primarily in West-Northwest and Midwest regions of the U.S. 

Salmonella is an organism that may cause fever, nausea, vomiting, abdominal pain and possibly bloody diarrhea in healthy individuals. It can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Consumers with these symptoms should consult their health care provider.
Fresh Express Precautionary Salad Recall- 10/11/12 (No other Fresh Express Salads are included in this recall)

BRAND	PRODUCT NAME	SIZE	UPC	Production Code	Best If Used By Date	POSSIBLE DISTRIBUTION STATES
Fresh Express	Hearts of Romaine	18 oz.	071279-262017	S270A24	OCT 11	AZ, AR, CA, CO, HI, ID, KS, LA, MN, MT, NV, NM, ND, OK, OR, TX, UT, WA, WI, WY

###

Dog Biscuits Recalled Due to Possible Salmonella Contamination

Dog Biscuits are being recalled due to possible Salmonella contamination.  There have been no reported illnesses.

 Nature's Recipe Voluntarily Recalls Nature's Recipe Oven Baked Biscuits With Real Chicken Due to Possible Salmonella Contamination
http://www.fda.gov/Safety/Recalls/ucm323823.htm?source=govdelivery

FOR IMMEDIATE RELEASE - October 13, 2012 - Nature’s Recipe brand is voluntarily recalling a limited supply of Nature’s Recipe® Oven Baked Biscuits with Real Chicken, manufactured in one of its U.S. production facilities. This is being done as a precautionary measure, as the product has the potential to be contaminated with Salmonella. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products.

Healthy people infected with Salmonella should monitor themselves for some, or all, of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected, but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

No pet or consumer illnesses from this product have been reported to date. However, because of its commitment to safety and quality, the Company is conducting a voluntary recall of this product.

The potentially affected lots of Nature’s Recipe Oven Baked Biscuits with Real Chicken were distributed nationally, primarily through pet specialty retailers.

Nature’s Recipe Oven Baked Biscuits with Real Chicken is sold in 19-ounce stand-up resealable pouches. The product affected by this recall is identified below and has the following "Best If Used By" dates:

Lot Code:	UPC Code:	Size:	Product Name/Description:	Best If Used By Date:
2199TP	30521 51549	19-ounces	Nature’s Recipe Oven Baked Biscuits with Real Chicken	10 11 13
2200TP	30521 51549	19-ounces	Nature’s Recipe Oven Baked Biscuits with Real Chicken	10 12 13

Product and product lots that do not appear on the list above are not subject to this recall.

Consumers who have purchased the above lots of Nature’s Recipe Oven Baked Biscuits with Real Chicken should stop feeding the product and discard immediately. For further information about the recall and for instructions on obtaining replacement product, consumers can use the Contact Us form at www.naturesrecipe.com1 or call the Consumer Hotline, 24 hours a day, at 800-237-3856.


About Nature’s Recipe®

Nature’s Recipe®, a brand of Del Monte Foods, markets a complete line of natural dog food and treats and recently introduced a line of natural cat food. Nature’s Recipe® has been making better pet food where “Every Ingredient Counts® ” for more than 30 years. For additional information about Nature’s Recipe®, visit www.naturesrecipe.com2. 

Sunland Recall Expands Again, Now Includes In-shell Peanuts

The Sunland Food Recall was once again expanded to include in-shell peanut products produced at their Peanut Processing Facility.  This expansion was done as part of the on-going investigation.  According to the CDC, there have been 35 illnesses linked to the Trader Joe brand of peanut butter.(http://www.cdc.gov/salmonella/bredeney-09-12/index.html).  No other products have been found to have caused illness, so the expansion of the recall is due to what investigators are discovering in the two plants.

Other companies also continue to recall products with products supplied by Sunland. (below)
 
Sunland, Inc. Announces Voluntary Extension of Ongoing Recall To Include Raw and Roasted Shelled and In-Shell Peanuts Due to Possible Health Risk
http://www.fda.gov/Safety/Recalls/ucm323824.htm?source=govdelivery


FOR IMMEDIATE RELEASE - October 12, 2012 - Sunland, Inc. today announced that it is extending its ongoing voluntary recall to include raw and roasted shelled and in-shell peanuts processed in its Peanut Processing Plant because the products have the potential to be contaminated with Salmonella. Specifically, the recall is being extended to include raw and roasted peanuts, both in-shell and shelled, which were processed in its Peanut Processing Plant located in Portales, New Mexico, and which are within their current shelf life or have no stated expiration date.

Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and those 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.

The original recall initiated by the Company on September 24, 2012, included peanut butter and other nut butter products produced in a separate building from where raw and roasted peanuts are processed. The reason for the initial voluntary recall was the potential for the recalled products to be contaminated with Salmonella. At that time, twenty-nine (29) people had reported Salmonella Bredeney PFGE matching illnesses in approximately eighteen (18) states, and of those who had been interviewed at that time, twelve of fourteen reported having eaten the same single product made by the Company. Since the recall was announced, additional confirmed illnesses have been reported. As of October 5, 2012, the total number of confirmed illnesses reported was thirty-five (35). The most current information available from the Centers for Disease Control and Prevention (CDC), regarding confirmed illnesses is available at their website: http://www.cdc.gov/salmonella/bredeney-09-12/index.html1

The extension being announced today is the result of the continued joint investigation by the Company and FDA. The Company has ceased the production and distribution of all products from both its Peanut Butter Plant and its Peanut Processing Plant while FDA and the Company continue their investigation.

The raw and roasted peanuts available to retail customers were distributed primarily under the Company’s own label and were distributed primarily to produce houses and nationally to numerous large supermarket, grocery and retail chains. The products also were available for purchase on the internet. The roasted and roasted/salted peanuts being recalled were distributed during the six month period prior to the recall date (April 12, 2012 – October 12, 2012), and will have best by/expiration dates on the packaging from October 12, 2012 through April 12, 2013. The raw peanuts being recalled (shelled and in-shell), were distributed during the twelve months prior to the recall date (October 12, 2011 – October 12, 2012), and will have either best by dates from October 12, 2012 through October 12, 2013 on the packaging, or a “Crop Year” marking on the package of 2011 or 2012, up to and including October 12, 2012.

Consumers who have purchased any of the recalled products are urged not to eat them and to return products to the place of purchase for a full refund or dispose of them immediately. The “Best-If-Used-By” date or product expiration date is printed on the packaging. The UPC used to identify the recalled products is located below the bar code on all products. In-shell peanuts that were sold in 2, 5 and 10 pound mesh bags (raw, roasted and salted/roasted), do not include an expiration date on the mesh bags. All such products should not be eaten and should be returned to the place of purchase for a full refund or disposed of immediately. All expired products should be discarded. Customers who purchased products directly from the Company’s website should discard the products and contact the Company at 1-866-837-1018.

Consumers can contact the Company at 1-866-837-1018 for information on the recall. This toll-free number is operational 24 hours a day.

The recall is being conducted in cooperation with the United States Food and Drug Administration (FDA). The most current information available from FDA is posted at the following website: http://www.fda.gov/Food/FoodSafety/CORENetwork/ucm320413.htm2

The specifics of the affected products are set forth below. Products being added to the list for the first time appear in the first table. All previously identified products follow in the second table.

Creative Energy Foods, Inc. Recalls Ridgebar Brand Nutrition Bars Due to Possible Health Risk Associated With Sunland Inc. Peanut Products
http://www.fda.gov/Safety/Recalls/ucm323818.htm?source=govdelivery

Due to Sunland Peanut Butter Recall, AdvancePierre Foods Initiates Voluntary Recall of Select Frozen Peanut Butter Products
http://www.fda.gov/Safety/Recalls/ucm323800.htm?source=govdelivery

Lin-Mar Partners Recalls Roasted Peanut With Chocolate and Peanut Butter Trail Longhorn Bars Because of Possible Health Risk
http://www.fda.gov/Safety/Recalls/ucm323803.htm?source=govdelivery

Purefit Inc. Announces Voluntary Recall of Purefit Peanut Butter Crunch Bars Because of Possible Salmonella Contamination
http://www.fda.gov/Safety/Recalls/ucm323825.htm?source=govdelivery

General Mills Voluntarily Recalls Limited Number of Cascadian Farm Snack Bars Containing Peanuts
http://www.fda.gov/Safety/Recalls/ucm323308.htm?source=govdelivery