The US surveillance system for tracking foodborne illnesses, or PulseNet, is 20 years old. Through time, the technology has improved and its reach is now global.
In the US, the system is comprised by a network of 83 laboratories linked to the CDC in Atlanta. Using genetic identification technology, including Whole Genome Sequencing or WGS, it can identify outbreak clusters through matching bacterial isolates involved in cases. This information is then used to help identify the source of the outbreak.
This article in EMBO is a nice summary of Pulsenet and how it has impacted food safety.
EMBO Reports
http://onlinelibrary.wiley.com/doi/10.15252/embr.201643128/full
Future challenges for tracking foodborne diseases
PulseNet, a 20-year-old US surveillance system for foodborne diseases, is expanding both globally and technologically
Authors - Efrain M Ribot and Kelly B Hise
Centers for Disease Control and Prevention, Atlanta, GA, USA
First published: 19 September 2016Full publication history
Monday, October 17, 2016
Turkey Products Recalled for Unidentified Black Substance
A Michigan establishment is recalling 54000 pounds of turkey products after a customer complaint was received for a black substance. This is a foodservice item so likely this was discovered by a retailer or foodservice operator. The black substance has not yet been identified.
USDA / FSIS Recall Notice
http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-097-2016-release
Michigan Turkey Producers Recalls Turkey Products Due To Possible Foreign Matter Contamination
Class I Recall 097-2016
Health Risk: High Oct 15, 2016
USDA / FSIS Recall Notice
http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-097-2016-release
Michigan Turkey Producers Recalls Turkey Products Due To Possible Foreign Matter Contamination
Class I Recall 097-2016
Health Risk: High Oct 15, 2016
Popcorn Chicken Recalled Because of Foreign Material
Tyson Foods New Holland, PA facility is recalling popcorn chicken nuggets packed due plastic pieces. According to the report - "The problem was discovered when the establishment received a consumer complaint from a school regarding foreign material, specifically hard plastic, found inside a bag of Tyson brand whole grain popcorn chicken product."
USDA News Release
http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-096-2016-release
Tyson Foods Recalls Frozen Popcorn Chicken Products Due To Possible Foreign Matter Contamination
Class I Recall 096-2016
Health Risk: High Oct 15, 2016
USDA News Release
http://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2016/recall-096-2016-release
Tyson Foods Recalls Frozen Popcorn Chicken Products Due To Possible Foreign Matter Contamination
Class I Recall 096-2016
Health Risk: High Oct 15, 2016
Friday, October 14, 2016
Venture Capitalist Start-Up, Soylent, Recalls Meal Replacement Due to Illnesses
A venture capitalist start-up nutrition company, Soylent, is recalling their nutrition snack bar after complaints of vomiting, diarrhea, and nausea.
First, who is buying this stuff? One look at the website and it looks like something a bunch of computer hipsters came up with. With all these real food companies with flat or decling sales, I am not sure why people feel that a bunch of techno-geeks can make a better product.
Second, the name....didn't they see the movie? Yeah, Soylent Green...that was a meal replacement too. But we all know what that was. And in case you don't, we'll let Charlton Heston tell you: https://www.youtube.com/watch?v=9IKVj4l5GU4
LA Times
http://www.latimes.com/business/technology/
Soylent stops selling nutrition bars after customers report diarrhea, other illnesses
by Paresh Dave
October 12, 2016
Meal replacement start-up Soylent halted sales of its new nutrition snack bar Wednesday and advised customers to discard any in their possession.
First, who is buying this stuff? One look at the website and it looks like something a bunch of computer hipsters came up with. With all these real food companies with flat or decling sales, I am not sure why people feel that a bunch of techno-geeks can make a better product.
Second, the name....didn't they see the movie? Yeah, Soylent Green...that was a meal replacement too. But we all know what that was. And in case you don't, we'll let Charlton Heston tell you: https://www.youtube.com/watch?v=9IKVj4l5GU4
LA Times
http://www.latimes.com/business/technology/
Soylent stops selling nutrition bars after customers report diarrhea, other illnesses
by Paresh Dave
October 12, 2016
Meal replacement start-up Soylent halted sales of its new nutrition snack bar Wednesday and advised customers to discard any in their possession.
Michigan Cheese Company Recalls Cheese Due to Supplier Listeria Issues
A Michigan company, Kuster's is recalling its institutional sized shredded, sliced and cubed cheese after the company was notified by their supplier, Farm Country Cheese, that there is the potential for Listeria contamination.
Farm County Cheese is no large industrial processor, quite the opposite. From the Farm County Cheese website:
Tradition ~ Heritage ~ CommunitySounds great, but if this is your supplier, are they controlling for Listeria? How about a FSMA required Supplier Preventive Control.
For over 25 years, Farm Country Cheese House has worked in partnership with our local Amish community to create fresh, antibiotic-free, artisanal cheeses. Located in Lakeview, Michigan (northeast of Grand Rapids), we are proud of the “family” of Amish farmers and workers who make up the majority of our staff. Our culture is supportive and kind, and we work together to bring the highest-quality and freshest cheese to you, our consumer.
Our cheeses are pure, simple, and clean. We use milk made by cows on our local Amish dairy farms, and follow Amish traditions and practices. Because the health and comfort of the cows is a top priority, the small dairy farms that we work with raise herds of only 4 to 20 cows, where each cow is hand-milked twice daily. In the operation of our equipment and business, we use minimal amounts of electricity, which is supplied to us by an electric cooperative.
FDA Recall Notice
Kuster's, Inc. Voluntarily Recalls Product Because Of Possible Health Risk
For Immediate Release
October 12, 2016
Warning Letter Issued to Company for Not Verifying That Corrective Measures Worked
FDA issued a Warning Letter to a California company after that company did not adequately respond to a 483 Report issued during inspection. The inspection was performed after the company's product was involved in a Salmonella outbreak. During the inspection, Salmonella was found during FDA environmental sampling and this was included as a finding on the FDA 483 that was issued. From the FDA website: "An FDA Form 483 is issued to firm management at the conclusion of an inspection when an investigator(s) has observed any conditions that in their judgement may constitute violations of the Food Drug and Cosmetic (FD&C)". The company is then expected to send a written response to the 483 report. "Companies are encouraged to respond to the FDA Form 483 in writing with their corrective action plan and then implement that corrective action plan expeditiously."
When a company does not properly respond and/or take appropriate corrective action, FDA will issue a Warning Letter. From the FDA website: "When it is consistent with the public protection responsibilities of the agency and depending on the nature of the violation, it is the Food and Drug Administration's (FDA's) practice to give individuals and firms an opportunity to take voluntary and prompt corrective action before it initiates an enforcement action. Warning Letters are issued to achieve voluntary compliance and to establish prior notice. (Prior notice is discussed in Chapter 10.) The use of Warning Letters and the prior notice policy are based on the expectation that most individuals and firms will voluntarily comply with the law."
As we have seen in a number of other recently issued Warning Letters (Examples 1, 2, 3, 4) companies are failing to properly address the elements of corrective action. As with this case, measures are taken, but the company fails to verify that those measures have worked. From this report: "However, you did not provide us with documentation demonstrating the effectiveness of these changes and any other changes you have made to prevent a reoccurrence of an outbreak." The verification that corrective measures worked is especially important after the company has had an outbreak and/or was found to have pathogen contamination issues.
FDA Warning Letter
http://www.fda.gov/ICECI/EnforcementActions/WarningLetters/2016/ucm524491.htm
WARNING LETTER
October 7, 2016
When a company does not properly respond and/or take appropriate corrective action, FDA will issue a Warning Letter. From the FDA website: "When it is consistent with the public protection responsibilities of the agency and depending on the nature of the violation, it is the Food and Drug Administration's (FDA's) practice to give individuals and firms an opportunity to take voluntary and prompt corrective action before it initiates an enforcement action. Warning Letters are issued to achieve voluntary compliance and to establish prior notice. (Prior notice is discussed in Chapter 10.) The use of Warning Letters and the prior notice policy are based on the expectation that most individuals and firms will voluntarily comply with the law."
As we have seen in a number of other recently issued Warning Letters (Examples 1, 2, 3, 4) companies are failing to properly address the elements of corrective action. As with this case, measures are taken, but the company fails to verify that those measures have worked. From this report: "However, you did not provide us with documentation demonstrating the effectiveness of these changes and any other changes you have made to prevent a reoccurrence of an outbreak." The verification that corrective measures worked is especially important after the company has had an outbreak and/or was found to have pathogen contamination issues.
FDA Warning Letter
http://www.fda.gov/ICECI/EnforcementActions/WarningLetters/2016/ucm524491.htm
WARNING LETTER
October 7, 2016
Thursday, October 13, 2016
Colors and Printing on Food Packaging
An article in Food Safety Magazine, Colorants in Food Packaging: FDA Safety Requirements (Oct/Nov 2016), reviews the FDA safety requirements of food packaging colors and printing. In summary, "The rules of thumb for determining the regulatory status of a pigment or dye are as follows: A substance that colors the food, even if it is in a packaging material, is a color additive and may be used only as permitted by an applicable FDA color additive regulation. Substances that color only a packaging material, and do not impart color to the food, are regulated as food additives if components of the substance are found to migrate into food. No premarket clearance by FDA is required, however, if the substance is not reasonably expected to become a component of food, is GRAS or is included on the list of “pre-1958 colorants.”
There are always questions about printing on the primary packaging and what is the concern. So, the primary question is whether that printing material can migrate to the food. If it can, then that color needs to be approved for use.
There are always questions about printing on the primary packaging and what is the concern. So, the primary question is whether that printing material can migrate to the food. If it can, then that color needs to be approved for use.
Tuesday, October 11, 2016
Blue Bell Expands Recall After Supplier Expands Recall of Cookie Dough, Blue Bunny and Others Also Issues Recalls
Blue Bell is expanding its recall of cookie dough ice cream after its ingredient supplier of cookie dough expanded its recall for Listeria. Just over two weeks ago, Blue Bell issued a recall for 5 lot codes of two flavors that contained the cookie dough ingredient. That recall now includes all product made from February 2, 2016 through September 7, 2016.
Along with this, Blue Bunny is recalling its Hoppin' Hollidoodle ice cream because it also contains the suspect cookie dough.
We have come to expect expansions of recalls when there is Listeria contamination issues. These recalls get expanded because the facility finds that there are underlying issues which indicate that Listeria could have been around for some time in the facility.
Other recalls affected by this supplier of cookie dough.
Chocolate Shoppe Ice Cream Company Recalls Select Products Containing Chocolate Chip Cookie Dough Pieces Purchased From Outside Supplier Aspen Hills Due To Possible Health Risk
Publix Recalls Publix Premium Chocolate Chip Cookie Dough Ice Cream Due To Possible Listeria monocytogenes Contamination From Aspen Hills, Inc. Cookie Dough Pieces
Nutrisystem Retail Division Voluntarily Recalls One Product Containing Chocolate Cookie Dough Pieces Purchased From Third Party Supplier Due To A Possible Health Risk
FDA Recall Notice
http://www.fda.gov/Safety/Recalls/ucm524749.htm
Outside Supplier Aspen Hills Expands Cookie Dough Recall; Blue Bell Recalls All Products Made With Aspen Hills Cookie Dough Due To Potential Health Risk
For Immediate Release
October 10, 2016
Along with this, Blue Bunny is recalling its Hoppin' Hollidoodle ice cream because it also contains the suspect cookie dough.
We have come to expect expansions of recalls when there is Listeria contamination issues. These recalls get expanded because the facility finds that there are underlying issues which indicate that Listeria could have been around for some time in the facility.
Other recalls affected by this supplier of cookie dough.
Chocolate Shoppe Ice Cream Company Recalls Select Products Containing Chocolate Chip Cookie Dough Pieces Purchased From Outside Supplier Aspen Hills Due To Possible Health Risk
Publix Recalls Publix Premium Chocolate Chip Cookie Dough Ice Cream Due To Possible Listeria monocytogenes Contamination From Aspen Hills, Inc. Cookie Dough Pieces
Nutrisystem Retail Division Voluntarily Recalls One Product Containing Chocolate Cookie Dough Pieces Purchased From Third Party Supplier Due To A Possible Health Risk
FDA Recall Notice
http://www.fda.gov/Safety/Recalls/ucm524749.htm
Outside Supplier Aspen Hills Expands Cookie Dough Recall; Blue Bell Recalls All Products Made With Aspen Hills Cookie Dough Due To Potential Health Risk
For Immediate Release
October 10, 2016
NY Taco Chain Linked to Over 150 Cases of Foodborne Illness
A NY taco chain is being linked to over 150 people becoming ill. Cases have occurred in two counties and it appears that a 'handful' of the Mighty Taco locations may be involved. The symptoms are nausea and vomiting. After removing suspect food, including refried beans, the number of cases looks to be subsiding.
An update was provided on 10/20/16.
WKBW News
http://www.wkbw.com/news/142-reported-illnesses-after-mighty-tacos-refried-beans-caused-concern-in-erie-county
142 reported illnesses after Mighty Taco's refried beans caused concern in Erie County
An update was provided on 10/20/16.
WKBW News
http://www.wkbw.com/news/142-reported-illnesses-after-mighty-tacos-refried-beans-caused-concern-in-erie-county
142 reported illnesses after Mighty Taco's refried beans caused concern in Erie County
Subscribe to:
Posts (Atom)