Unfortunate Disconnect Between Supplier and Retailer Leads to Death Due to Undeclared Peanuts

Tragic stories bring home the importance of preventing simple errors such as getting proper labels on packages.  In a most recent case, a 25 year old world-class dancer "tragically lost her life due to anaphylactic shock resulting from a severe allergic reaction to a cookie manufactured by Cookies United and sold by the supermarket chain Stew Leonard's. The FDA and Stew Leonard's issued a recall of the Vanilla Florentine Cookies that were sold at Stew Leonard's in Danbury and Newington, CT from November 6 – December 31, 2023.  The cookie contained peanuts which were not listed as part of the ingredients."

Unfortunately for Steward Leonards, they were made aware of the inclusion of peanuts earlier in the year, but failed to update their label.  From Cookies United Press Release "Stew Leonard’s claimed in an earlier press release that “The cookies contain peanuts, which was an ingredient not disclosed to Stew Leonard’s by the manufacturer.” [bold is ours]  Unfortunately, considering the tragedy of these circumstances, we need to point out that Stew Leonard’s was notified by Cookies United in July of 2023 that this product now contains peanuts and all products shipped to them have been labeled accordingly.  This product is sold under the Stew Leonard’s brand and repackaged at their facilities.  The incorrect label was created by, and applied to, their product by Stew Leonard’s."

A very unfortunate disconnect between the supplier and the retailer.

Update on Lead Contamination in Applesauce Pouches (1/30/24)

FDA and CDC provided updates (1/30/24 and 1/26/24 respectfully) on the lead contamination issue in apple cinnamon fruit pouches.  CDC has received reports of 98 confirmed cases, 269 probable cases, and 37 suspected cases for a total of 404 cases from 43 different states through their reporting structure.  (FDA is reporting 90 reported cases).  This number of reported cases is up 88 cases from the Jan 5, 2024 update.

"FDA has no indication that this issue extends beyond these recalled products and does not have any confirmed reports of illnesses or elevated blood lead level adverse events reported for other cinnamon-containing products or cinnamon.  As of January 29, 2024, FDA has not received any additional confirmed complaints/reports of adverse events potentially linked to recalled product."

FDA’s investigation is ongoing to determine the point of contamination and whether additional products are linked to illnesses


https://www.fda.gov/food/outbreaks-foodborne-illness/investigation-elevated-lead-chromium-levels-cinnamon-applesauce-pouches-november-2023?utm_medium=email&utm_source=govdelivery
Investigation of Elevated Lead & Chromium Levels: Cinnamon Applesauce Pouches (November 2023)
Current Update
January 30, 2024

FDA has no indication that this issue extends beyond these recalled products and does not have any confirmed reports of illnesses or elevated blood lead level adverse events reported for other cinnamon-containing products or cinnamon.

Favorite Research Paper Award Discusses Salmonella and Wild Birds

What is your favorite clinical microbiology research paper form 2023? Not a question I have ever been asked or even thought about. Favorite movie or favorite restaurant visit, sure, but can't say I have a favorite clinical microbiology paper. Well some microbiology geeks picked a paper authored by one of our favorite Penn State microbiology geeks, Dr. Ed Dudley's research paper as their favorite paper. Awesome. Congrats to him and his collaborators. And to the editors point, it has a lot going for it ....Salmonella, wild birds, evolution, and One Health.  We can think about this as it relates to food in that wild birds are a source of Salmonella within the food supply chain.

The selection by Editors in Conversation, Journal of Clinical Microbiology
https://lnkd.in/eHd4hZwz

Starting around minute 39
So what is this paper...

Whole-Genome Subtyping Reveals Population Structure and Host Adaptation of Salmonella Typhimurium from Wild Birds
https://journals.asm.org/doi/10.1128/jcm.01847-22

ABSTRACT

Within-host evolution of bacterial pathogens can lead to host-associated variants of the same species or serovar. Identification and characterization of closely related variants from diverse host species are crucial to public health and host-pathogen adaptation research. However, the work remained largely underexplored at a strain level until the advent of whole-genome sequencing (WGS). Here, we performed WGS-based subtyping and analyses of Salmonella enterica serovar Typhimurium (n = 787) from different wild birds across 18 countries over a 75-year period. We revealed seven avian host-associated S. Typhimurium variants/lineages. These lineages emerged globally over short timescales and presented genetic features distinct from S. Typhimurium lineages circulating among humans and domestic animals. We further showed that, in terms of virulence, host adaptation of these variants was driven by genome degradation. Our results provide a snapshot of the population structure and genetic diversity of S. Typhimurium within avian hosts. We also demonstrate the value of WGS-based subtyping and analyses in unravelling closely related variants at the strain level.

An selected items from the paper as it impacts food.

"As indicated in this study, wild animals such as wild birds represent remarkable but less studied reservoirs for emerging variants of bacterial pathogens. Epidemiologic studies have also revealed a correlation between some human and avian salmonellosis outbreaks, suggesting transmission of bacterial pathogens between wild birds and humans (55–59). Although such transmission is rare relative to transmission between humans and humans or between humans and domestic animals (72, 73), they can still have a substantial impact on global health as avian hosts are highly mobile and possibly carry and spread bacterial pathogens over large distances (44, 45). In a One Health framework, current surveillance of bacterial pathogens needs to be focused not only on clinical isolates or isolates from domestic animals but also on those originating from wild animals."

CDC - Salmonella Outbreak Associated with Cantaloupes is Over, 407 Reported Cases

CDC released notice that the 2023 Salmonella outbreak linked to cantaloupes is over.  Cases were first identified in October 2023, with recalls being issued in November, 2023 by SOFIA PRODUCE, LLC, of Nogales, Arizona which does business under the name “Trufresh”.

FDA testing did link the company to the outbreak, but little additional information from the investigation was found.





https://www.cdc.gov/salmonella/sundsvall-11-23/index.html

Salmonella Outbreak Linked to Cantaloupes
January 19, 2024
This outbreak is over

Fast Facts
Illnesses: 407
Hospitalizations: 158
Deaths: 6
States: 44
Recall: Yes

PA Distributor Recalls Dried Mango for Undeclared Sulfites

TRUONG GIANG DISTRIBUTOR CORP of Philadelphia, PA is recalling Golden Owl Dried Mango, because it may contain undeclared sulfites.   The recall was initiated after routine sampling by the New York State Department of Agriculture and Markets found sulfites in the product which was distributed in packaging that did not reveal the presence of sulfites. Subsequent investigation indicates the problem was caused by a temporary breakdown in the supplier’s labeling processes.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/truong-giang-distributor-corp-issues-allergy-alert-undeclared-sulfites-dried-mango
Truong Giang Distributor Corp Issues Allergy Alert on Undeclared Sulfites in Dried Mango
Summary
Company Announcement Date: January 29, 2024
FDA Publish Date:  January 29, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared sulfites.
Company Name:  TRUONG GIANG DISTRIBUTOR CORP
Brand Name:  Golden Owl
Product Description:  Dried mango

Can Kiwifruit Improve Your Mood?

Can Kiwifruit improve your mood?  "In a study, published in The British Journal of Nutrition, researchers found the furry fruit improved vitality and mood in as little as four days."  Just two kiwifruit per day was better than the vitamin C placebo. 

"Vitamin C intake has been associated with improved mood, vitality, well-being, and lower depression, while vitamin C deficiency is associated with higher depression and cognitive impairment.  Participants took daily either a vitamin C supplement, placebo, or two kiwifruit. They then reported their vitality, mood, flourishing, sleep quality, sleep quantity, and physical activity using smartphone surveys.  The researchers found kiwifruit supplementation improved vitality and mood within four days, peaking around 14–16 days, and improved flourishing from day 14. Vitamin C, on the other hand, marginally improved mood until day 12."

This research was funded by the University of Otago [New Zealand University] and Zespri International [a kiwifruit grower cooperative].

https://www.otago.ac.nz/news/newsroom/furry-fruit-improves-mental-health-fast
Furry fruit improves mental health – fast
25 January 2024

Kiwifruit has proven itself as a powerful mood booster and new research from the University of Otago has shown just how fast its effects can be.

France - Gourmet Christmas Party Source for 700 Cases of Norovirus Infection

Many of us do not get the opportunity to attend those fancy company Holiday parties where gourmet food is served.  Well, here is one party you should be happy you were left off the invite list.  In France, Airbus held a Christmas party for its employees where 700 of them came down with Norovirus infection

"Jean-Claude Iribarren, the secretary of the Airbus Atlantic works committee, told the paper the food had been prepared by the company’s canteen. “As we do every year, we organised a Christmas dinner for 2,600 people with a lot of local suppliers,” he said."

Unfortunately, for 700 of them, they became sick with vomiting and diarrhea. "The affected workers showed “clinical signs of vomiting and/or diarrhoea” after the seasonal dinner on 14 December. Most fell ill within 24 to 48 hours after the meal.

https://www.theguardian.com/business/2023/dec/23/airbus-atlantic-staff-christmas-dinner-gastroenteritis-outbreak
‘Worse than giving birth’: 700 fall sick after Airbus staff Christmas dinner

French health authorities investigating mass gastroenteritis outbreak after company restaurant served foie gras and lobster

Potato Chip Manufacturer Recalls Mis-bagged Chips Resulting in Allergen Recall

Utz Quality Foods, LLC., is issuing a voluntary recall for 88 cases of Utz® 2.75 oz. Wavy Original Potato Chips due to an undeclared milk allergen. This recall was initiated after Utz learned that approximately 1200 single-serve bags contained Utz® Wavy Original Potato Chips flavored with seasoning instead of plain Utz® Wavy Original Potato Chips.  The items subject to this voluntary recall were distributed to retail outlets only in New York State and primarily within New York City

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/utz-quality-foods-issues-allergy-alert-undeclared-milk-utzr-wavy-original-potato-chips-metro-new
Utz Quality Foods Issues Allergy Alert on Undeclared Milk in Utz® Wavy Original Potato Chips in Metro New York Area
Summary
Company Announcement Date:  January 25, 2024
FDA Publish Date:  January 26, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared milk allergen
Company Name:  UTZ Quality Foods
Brand Name:  UTZ
Product Description:  Utz 2.75 oz. Wavy Original Potato Chips

Company Announcement

HANOVER, PA. (BUSINESS WIRE) – Utz Quality Foods, LLC., is issuing a voluntary recall for 88 cases of Utz® 2.75 oz. Wavy Original Potato Chips due to an undeclared milk allergen. This recall was initiated after Utz learned that approximately 1200 single-serve bags contained Utz® Wavy Original Potato Chips flavored with seasoning instead of plain Utz® Wavy Original Potato Chips. People who have an allergy or severe sensitivity to milk may run the risk of an allergic reaction if they consume these products.

Oregon Firm Recalls Yogurt Yogurt Product for Undeclared Allergens

Al Amir Fresh Foods of Milwaukie, Oregon is recalling Al Amir brand hummus dip products due to undeclared sesame and Tzatziki Cucumber Yogurt due to undeclared milk.   The recall was initiated after it was discovered that Al Amir hummus labels declare tahini but do not declare sesame and Tzatziki Cucumber Yogurt label declares sour cream & yogurt but does not declare milk. 

I guess the company never got the memo that allergen labeling was required on food products.

htps://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/al-amir-fresh-foods-issues-allergy-alert-undeclared-sesame-hummus-dip-products-and-undeclared-milk
Al Amir Fresh Foods Issues Allergy Alert on Undeclared Sesame in Hummus Dip Products and Undeclared Milk in Tzatziki Cucumber Yogurt
Summary
Company Announcement Date:  January 19, 2024
FDA Publish Date:  January 20, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared Sesame & Milk
Company Name:  Al Amir Fresh Foods
Brand Name:  Al Amir Fresh Foods
Product Description:  Hummus Dip & Tzatziki Cucumber Yogurt

NY Distributor Recalls Dried Plum Products due to Undeclared Sulfites

Rong Shing Trading NY Inc., 47-57 Bridgewater Street, Brooklyn, NY is recalling its 4.7oz (135g) packages of “Lian Sheng Dried Tangerine Plum”  and 5.8oz (165g) packages of “Lian Sheng Dried Plum” because they contain undeclared sulfites. (2 separate recalls)  The recall was initiated after routine sampling by Florida Department of Agriculture and Consumer Services and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in the products.  The consumption of 10 milligrams of sulfites per serving could occur in certain sulfite sensitive individuals upon ingesting 10 milligrams or more of sulfites. Analysis of the Dried Tangerine Plum revealed they contained 21.91

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/rong-shing-trading-ny-inc-issues-alert-undeclared-sulfites-lian-sheng-dried-plum
Rong Shing Trading NY Inc. Issues Alert on Undeclared Sulfites in “Lian Sheng Dried Plum”
Summary
Company Announcement Date: December 14, 2023
FDA Publish Date: January 19, 2024
Product Type: Food & Beverages
Reason for Announcement: Undeclared Allergen-Undeclare Sulfites
Company Name: RONG SHING
Brand Name: Lian Sheng
Product Description: Dried Plum

USDA FSIS Issues Public Health Alert for NY Establishment's Raw Pork Dumpling Product Produced Without Federal Inspection

USDA-FSIS issued a Public Health Alert for raw frozen dumpling product "because Dim Sum Factory Inc., a Flushing, N.Y., establishment, produced and distributed raw, frozen pork dumpling products without the benefit of federal inspection."  The problem was discovered during routine FSIS surveillance activities. FSIS determined that the location where the pork wonton products were being produced were not on the official premises of the establishment and, therefore, were not inspected.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-raw-frozen-pork-dumpling-products-produced-without
FSIS Issues Public Health Alert for Raw Frozen Pork Dumpling Products Produced without Benefit of Inspection

DIM SUM FACTORY, INC.

FSIS Announcement

WASHINGTON, Jan. 18, 2024 - The U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) is issuing a public health alert because Dim Sum Factory Inc., a Flushing, N.Y., establishment, produced and distributed raw, frozen pork dumpling products without the benefit of federal inspection. A recall was not requested because the products are no longer available for purchase.

USDA Issues Health Alert After Additional Cases of Salmonella Infection Reported from Recalled Charcuterie Meat Products

USDA issued a Health Alert for charcuterie meats, Busseto brand Charcuterie Sampler and Fratelli Beretta brand Antipasto Gran Beretta manufactured by Fratelli Beretta in Mount Olive NJ as CDC issued an update that shows there were additional new cases of Salmonella infection The recall was initially posted on January 5, 2024, but there are now 23 new cases, now totaling 47 cases in 22 different states.

The reason for ongoing cases is that many people still have the product.  Although the retailers pulled it from the shelf, many probably had it stowed away in their refrigerator or freezer.  





https://www.cdc.gov/salmonella/charcuterie-meats-01-24/index.html
Salmonella Outbreak Linked to Charcuterie Meats
Posted January 18, 2024

Fast Facts
Illnesses: 47 (23 new)
Hospitalizations: 10 (5 new)
Deaths: 0 (0 new)
States: 22 (8 new)
Recall: Yes
Investigation status: Active (first posted on January 5, 2024).

MA Retailer Recalls Salad After Mislabeling Issue Results in Undeclared Allergens

Hans Kissle of Haverhill, MA, is recalling its 7-ounce packages of MEXICAN STYLE QUINOA SALAD, deli salad, because the product contains undeclared egg and soy.  The recalled MEXICAN STYLE QUINOA SALAD was distributed to Hannaford’s Supermarkets in the following states MA, NH, NY, ME, and VT.  The recall was initiated after it was discovered that the product was mislabeled and distributed in packaging that did not declare the presence of egg or soy.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hans-kissle-issues-allergy-alert-undeclared-soy-egg-hans-kissle-mexican-style-quinoa-salad
Hans Kissle Issues Allergy Alert on Undeclared Soy & Egg in "Hans Kissle Mexican Style Quinoa Salad"
Summary
Company Announcement Date:  January 18, 2024
FDA Publish Date:  January 18, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared Allergens – Egg, Soy
Company Name:  Hans Kissle
Brand Name:  No Brand
Product Description:  Mexican Style Quinoa Salad

Virginia Company Recalls Nut Mix Containing Party Mix Resulting in Undeclared Allergens

Whitley’s Peanut Factory of Hayes, Virginia is recalling 12oz Deluxe Nut Mix with specific code dates because they may contain undeclared peanuts, milk, soy, wheat, and sesame.  The recall of this product was initiated after the Quality Assurance Department became aware of a limited number of 10.5oz Whit’s Party Mix tins labeled with 12oz Deluxe Nut Mix labels. The depth of the recall has been expanded to include the previous production date through the time in which the company became aware of the issue. While both products contain almonds, Whit’s Party Mix also includes peanuts, milk, soy, wheat, and sesame which are not listed in the “Contains” statement of the Deluxe Nut Mix label.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/whitleys-peanut-factory-issues-allergy-alert-undeclared-peanuts-milk-soy-wheat-and-sesame-limited
Whitley’s Peanut Factory Issues an Allergy Alert on Undeclared Peanuts, Milk, Soy, Wheat, and Sesame for Limited Units of Deluxe Nut Mix 12oz (340g)
Summary
Company Announcement Date:  January 18, 2024
FDA Publish Date:  January 18, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared Allergens - Peanuts, Milk, Soy, Wheat, and Sesame
Company Name:  Whitley’s Peanut Factory
Brand Name:  Whitley’s Peanut Factory
Product Description:  Deluxe Nut Mix

Tianeptine (aka Drug Store Heroin) and the Supplement Industry

An article in Natural Products Insider discusses tianeptine, aka drug store heroin, and the connection being made to the supplement industry.  Tianeptine, an antidepressent, and according to the Cleveland Clinic, "It enhances a person’s mood by binding to the brain’s opioid receptors — just like heroin, morphine and other narcotics. Experts quickly discovered that it was highly addictive, as patients began doctor-shopping for more and were developing withdrawals after abruptly stopping it.” The U.S. Food and Drug Administration (FDA) has never approved tianeptine to treat depression or any other condition. Tianeptine also never earned a Generally Recognized as Safe (GRAS) designation, a label the FDA puts on some chemicals and food additives.  But some companies found a legal loophole that allowed them to put tianeptine in products labeled as “dietary supplements.” That’s why you can still find it on store shelves today. Tianeptine appears in various so-called supplements, often those sold at convenience stores and gas stations. ""

Further, "The FDA doesn’t strictly regulate dietary supplements or approve them before they’re sold. But they have tracked down and sent warning letters to companies that sell tianeptine products. And some states have banned tianeptine, including: Alabama. Georgia. Indiana. Kentucky. Michigan. Mississippi. Ohio. Tennessee.

So the article discusses the impact on the supplement industry, which is far less regulated than the medical industry and even the food industry.  I don't agree in that this does not further damage the supplement industry, but provides another indicator of how unregulated the industry is.


Natural Products Insider
https://www.naturalproductsinsider.com/supplement-regulations/tianeptine-sales-besmirch-supplement-industry-s-reputation-but-who-is-really-at-fault-?
Tianeptine sales besmirch supplement industry’s reputation, but who is really at fault?
A shadowy network supplies products featuring illegal drugs that are sold in convenience and liquor stores and smoke shops. Is that the fault of the dietary supplement industry?
Hank Schultz
January 12, 2024

NJ CEA Farm Recalls Spinach After State Lab Finds Listeria

BrightFarms has issued a voluntary recall of spinach grown by its supplier Element Farms in their Pompton Plains, New Jersey farm and distributed under the BrightFarms brand because the spinach has the potential to be contaminated with Listeria monocytogenes. Due to potential cross-contamination, BrightFarms is also issuing a voluntary recall of a limited quantity of four salad kit products (shown below) from its Selinsgrove, PA facility.  The recall of spinach was initiated after routine sampling conducted by Element Farms yielded a positive result for Listeria monocytogenes. Due to potential cross-contamination at BrightFarms’s Selinsgrove, Pennsylvania facility, BrightFarms is also recalling a limited quantity of four select salad kit products. No positive test results or reported illness have been received on those products, to date.  As a result of today’s recall, the company has temporarily suspended distribution of Element Farms grown spinach.

This product is grown as under CEA, or Controlled Environmental Agriculture.  From the Element Farms website, the company "is a sustainable farm based in Lafayette, NJ." They  grow the " greens hydroponically  and without pesticides in a controlled-agriculture environment".  The "greens start out in a sterile soil/peat moss and then are moved to large ponds of ultra-filtered water to grow hydroponically".

Interesting is this from the website:
Do I need to wash your greens?

No. Our greens are grown indoors without pesticides, herbicides, and fungicides, and away from the outdoor contaminants that plague field farmers. We personally don’t wash our greens before eating--that’s another benefit to growing them in an ultra-pure environment--but you’re always welcome to. We don’t pre-wash our greens so they stay as fresh as can be in your clamshell.
A note on other brands’ triple-washed greens: triple-washed greens are most often washed in a chlorine solution and should be washed again at home before eating."

The question here is how did Listeria get into the production system.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/brightfarms-recalls-spinach-and-salad-kits-because-possible-health-risk-result-supplier-element
Brightfarms Recalls Spinach and Salad Kits Because of Possible Health Risk as a Result of Supplier Element Farms Recall
Summary
Company Announcement Date:  January 17, 2024
FDA Publish Date:  January 17, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Potential Foodborne Illness-Listeria monocytogenes
Company Name:  BrightFarms
Brand Name:  BrightFarms
Product Description:  Spinach and Salad Kits

Imported Indian Ingredient Recalls for Undeclared Wheat Even Though Stated on Precautionary Label

Kinjin Food Pvt. Ltd. Maharashtra, India is recalling its 50 gm, 100 gm, 200 gm & 500 gm, 1 Kg packages of "Asafoetida” Vandevi Yellow powder because they may contain undeclared traces wheat.  The recall was initiated after it was discovered that the product was being manufactured at a plant which also processed wheat products and therefore, there may be a possibility that the product may contain undeclared traces of wheat and the packaging did not mention the presence of traces of wheat as per the declaration required under labelling requirements of FSMA. Subsequent investigation indicates the problem was caused due to misunderstanding of the precautionary labelling done on the product however not as per the labelling requirement of FSMA.

So basically, the foreign company producing the product thought it was acceptable to have trace amounts in the product (a function of inadequate cleaning / product protection) if they had the precautionary label on the product.  As we know, the Precautionary Label does not allow one to process without adequate allergen controls.

What is Asafoetida?  From bon appetit, "It is essentially a gum resin extracted from ferula, an herb in the celery family. It is usually available as a coarse yellow powder and smells like boiled eggs because of its sulfur compounds—which explains one of its other nicknames, devil’s dung. But don’t be put off by the pungency. When used properly, a pinch of hing supercharges every other spice in the pan, like salt but in a funkier way (and without any sodium)."

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kinjin-food-pvt-ltd-maharashtra-india-issues-allergy-alert-undeclared-wheat-traces-vandevi
Kinjin Food Pvt Ltd, Maharashtra, India Issues Allergy Alert on Undeclared Wheat Traces in "Vandevi Asafoeitida Yellow Powder"
Summary
Company Announcement Date:  January 10, 2024
FDA Publish Date:  January 17, 2024
Product Type:  Food & Beverages
Reason for Announcement:  May contain undeclared wheat traces.
Company Name:  Kinjin Food Pvt. Ltd.
Brand Name:  Vandevi
Product Description:  Asafoetida Yellow Powder in 50 gram, 100 gram, 200 gram, 500 gram, and 1 kilogram packages.

Hawaii Retailer Recalls Mislabeled Nut Brownies With Undeclared Peanuts

Big Island Candies of Hilo, Hawaii is voluntarily recalling 120 boxes of their Makana Brownie Assortment Box (batch 60) purchased from its Ala Moana Store because the product contains undeclared peanuts.  A portion of the box may contain Milk Chocolate Covered Peanut Butter Brownies instead of Milk Chocolate Covered Macadamia Nut Brownies. The label does not depict peanut as a key ingredient.  This recall was initiated as a result of information received by a consumer who had an adverse reaction. To date, no other incidents have been reported. Subsequent investigation indicates the problem was caused at the packing and labeling stage and was limited to batch 60 of this item.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/big-island-candies-issues-allergen-alert-undeclared-peanuts-makana-brownie-assortment
Big Island Candies Issues Allergen Alert on Undeclared Peanuts in “Makana Brownie Assortment”
Summary
Company Announcement Date:  January 16, 2024
FDA Publish Date:  January 17, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Contains undeclared peanuts
Company Name:  Big Island Candies
Brand Name:  Big Island Candies
Product Description:  Brownie Assortment

CA Company Recalls Aged Cotija Mexican Grating Cheese After State Lab Finds Listeria

Rizo Lopez Foods, Inc. of Modesto, CA is recalling 344 cases of Aged Cotija Mexican Grating Cheese (8oz) because it has the potential to be contaminated with Listeria monocytogenes.  The recall was a result of a routine sampling program by the Hawaii State Department of Health’s Food and Drug Branch on Wednesday, January 3rd which revealed that the finished product contained the bacteria.

To date, no confirmed illnesses related to this product have been reported.

Aged Cotija Mexican Grating Cheese (8oz) was distributed nationwide through distributors.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/rizo-lopez-foods-inc-recalls-aged-cotija-mexican-grating-cheese-8oz-because-possible-health-risk
Rizo Lopez Foods, Inc. Recalls Aged Cotija Mexican Grating Cheese (8oz) Because of Possible Health Risk
Summary
Company Announcement Date:  January 11, 2024
FDA Publish Date:  January 11, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Potential Listeria monocytogenes contamination.
Company Name:  Rizo Lopez Foods, Inc.
Brand Name:  Rio Bros California Creamery
Product Description:  Aged Cojita Mexican Grating Cheese

CA Company Recalls Jelly Bars Due to Potential Choking Hazard

U.S. Trading Company of Hayward, CA is recalling Dragonfly jelly bars because it contains konjac powder and may present a choking hazard.  The recall was initiated after New York State Agriculture Department of Agriculture and Markets collected a sample of the jelly containing Konjac. Based upon the products containing the ingredient konjac and the dimensions, FDA has determined that the products present a choking hazard.

Konjac and its consequent texture and consistency could pose a choking hazard to small children as well as adults with functional and/or anatomic abnormalities.  The recalled Jelly bars were distributed to retailers Nationwide.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/us-trading-company-hayward-ca-recalling-dragonfly-jelly-bars-because-it-contains-konjac-powder-and
U.S. Trading Company of Hayward, CA is Recalling Dragonfly Jelly Bars Because it Contains Konjac Powder and May Present a Choking Hazard
Summary
Company Announcement Date:  January 11, 2024
FDA Publish Date:  January 11, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Product contains konjac powder and may present a choking hazard.
Company Name:  U.S. Trading Company
Brand Name:  Dragonfly
Product Description:  Jelly Handbag and Jelly Backpack containing Jelly Bars

Quaker Oats Company Expands Recall to Include Cereals and Snack Bars Due to Potential Salmonella Contamination

The Quaker Oats Company expanded their  December 15, 2023 recall of granola products due to potential Salmonella contamination to include additional cereals, bars and snacks.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/update-quaker-issues-revised-recall-notice-additional-products-due-possible-health-risk
Update: Quaker Issues Revised Recall Notice with Additional Products Due to Possible Health Risk
Summary
Company Announcement Date:  January 11, 2024
FDA Publish Date:  January 11, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Potential for Salmonella contamination
Company Name:  The Quaker Oats Company
Brand Name:  Multiple brand names
Product Description:  Cereal, bars, and snacks

FDA Issues First Annual CORE Report Summarizing FDA Investigations Into Foodborne Outbreaks

The FDA issued the first CORE (Coordinated Outbreak Response & Evaluation Network) annual report summarizing the investigations of foodborne outbreaks and adverse events in FDA-regulated human foods for the 2022 calendar year.

"The FDA’s CORE Network was established in 2011 with the mission to find, stop, and aid in the prevention of foodborne illness outbreaks. This is accomplished through disease surveillance, outbreak response, post-response activities, and collaboration with CDC and state and local public health agencies. Every year, CORE evaluates and responds to numerous foodborne outbreaks related to FDA-regulated products."

"In 2022, CORE evaluated 65 incidents, responded to 28, and issued advisories for 11. These numbers show a slight increase in the number of incidents evaluated in recent years, with 59 incidents evaluated, 19 responses, and 10 advisories issued in 2021. The investigations in 2022 included E. coli, Cronobacter, hepatitis A virus, Listeria monocytogenes, and Salmonella which were linked to a variety of products, including produce, dairy, and fish."

The 2022 annual report highlights a few noteworthy outbreaks from 2022: Listeria monocytogenes linked to enoki mushrooms, Salmonella linked to cantaloupe, and Salmonella linked to peanut butter.

In our reporting, we summarized the FDA findings of these noteworthy outbreaks: 

Salmonella in Cantaloupe (August 2022) - The investigation did not find a definitive source for the Salmonella strain found in the outbreak, although a common  packinghouse was identified.  The report does give some broad recommendations that packing houses, as well as farms, should be following.   Key among these, from my perspective, developing written procedures (SOPs) for the operation based upon reducing risk and then following these procedures with documentation.  It seems that this was the biggest knock against the firm in this investigation.

Salmonella in Peanut Butter (May 2022)  Inspectors found "found serious violations of the Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food regulation" and "failure of the owner, operator, or agent in charge of a covered facility to comply with the preventive controls provisions of the CGMP & PC rule"  The biggest issue was related to positive tests in the facility and the corrective action that was taken,  FDA finished the report stating the concern that Salmonella may be a resident contaminate within the facility and that broader measures are needed.

FDA published a strategy summary to prevent Listeria from Enoki mushrooms. 

The report provides links to the other FDA actions related to outbreaks.

LINK to report.

https://www.fda.gov/food/cfsan-constituent-updates/fda-releases-core-2022-annual-report-investigations-foodborne-outbreaks-and-adverse-events-fda
FDA Releases the CORE 2022 Annual Report: Investigations of Foodborne Outbreaks and Adverse Events in FDA-Regulated Foods

FDA and CDC Provide Update on Lead-in-Apple Sauce Contamination - Additional Reported Cases and the Finding of Chromium in Product

In a January 5, 2024 update to the lead contamination issue linked to cinnamon apple sauce product produced in Ec . and sold under the WanaBana Brand as well as by retailers Schnucks and Weis in the US, CDC is reporting that there are 321 reported cases. FDA states that as of Jan, 8, 2024, 87 of these cases have been confirmed. These cases range from zero and 53 years of age and the median age is one year old. (CDC’s case definition for state partners includes a blood lead level of 3.5 µg/dL or higher measured within 3 months after consuming a recalled WanaBana, Schnucks, or Weis brand fruit puree product after November 2022. As of January 5, CDC has received reports of 86 confirmed cases, 209 probable cases, and 26 suspected cases for a total of 321 cases from 38 different states through their reporting structure.)

FDA is also reporting that in their testing of the recalled products and the cinnamon collected from the Austrofoods facility, the agency has found chromium. People who ate recalled products, especially if they had elevated blood lead levels, may have been exposed to chromium.

From the FDA report, "Chromium is a naturally occurring element. It is an essential trace nutrient important to the diet that exists predominantly in two forms, chromium (III) and chromium (VI). Chromium (VI) is more toxic than chromium (III). Due to limitations in available testing methods, FDA was not able to definitively determine the form of chromium in the cinnamon apple puree sample (i.e., whether the chromium present is chromium (III) or chromium (VI)). The lead-to-chromium ratio in the cinnamon apple puree sample is consistent with that of lead chromate (PbCrO4) (which contains chromium (VI)), but this is not a definitive indicator that lead chromate or chromium (VI) (the more toxic form of chromium) was present. Information on the health effects of eating food contaminated with chromium (VI) are limited. The chromium in lead chromate may also be converted to chromium (III) (the less toxic form of chromium) due to the acidity of the applesauce and the stomach."

This was first reported in October of 2023 and FDA/CDC have provided updates over time.

https://www.fda.gov/food/outbreaks-foodborne-illness/investigation-elevated-lead-chromium-levels-cinnamon-applesauce-pouches-november-2023
Investigation of Elevated Lead & Chromium Levels: Cinnamon Applesauce Pouches (November 2023)
Current Update
January 9, 2024

As of January 8, 2024, FDA has received 87 confirmed complaints/reports of adverse events potentially linked to recalled product. To date, confirmed complainants, or people for whom a complaint or adverse event was submitted and met FDA’s complainant definition, are between zero and 53 years of age and the median age is one year old.

Retailer Recalls Oat Cookies After Formulation Issue Results in Undeclared Wheat

Wegmans has initiated a voluntary recall of Outrageous Oat Cookies purchased from its in-store bakeries starting on January 3, 2024, because they may contain undeclared wheat.  The recall was initiated when it was learned that a wheat-containing ingredient was inadvertently included in the product. There have been no reported injuries or illnesses to date associated with this recall. 

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/wegmans-food-markets-inc-issues-allergy-alert-outrageous-oat-cookies-undeclared-wheat
Wegmans Food Markets, Inc. Issues Allergy Alert on Outrageous Oat Cookies for Undeclared Wheat
Summary
Company Announcement Date:  January 10, 2024
FDA Publish Date:  January 10, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared wheat
Company Name:  Wegmans
Brand Name: Wegmans
Product Description:  Outrageous Oat Cookies

Wisconsin Establishment Recalls Kielbasa Product After Complaints for Bone Pieces in Product

Salm Partners, LLC, a Denmark, Wis. establishment, is recalling approximately 133,039 pounds of ready-to-eat turkey kielbasa products that may be contaminated with extraneous materials, specifically bone material.  The problem was discovered after the firm notified FSIS that it had received consumer complaints reporting that pieces of bone were found in the turkey kielbasa product. In addition, FSIS received two consumer complaints regarding this issue.

https://www.fsis.usda.gov/recalls-alerts/salm-partners-llc-recalls-ready-eat-turkey-kielbasa-products-due-possible-extraneous
Salm Partners, LLC Recalls Ready-to-Eat Turkey Kielbasa Products Due to Possible Extraneous Material Contamination

FSIS Announcement

WASHINGTON, Jan. 5, 2024 – Salm Partners, LLC, a Denmark, Wis. establishment, is recalling approximately 133,039 pounds of ready-to-eat turkey kielbasa products that may be contaminated with extraneous materials, specifically bone fragments, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

USDA Issues Public Health Alert for Frozen Mushroom Risotto Products After Incorrect Packaging of Hot Dogs in Puff Pastry Results in Undeclared Allergen

USDA-FSIS issued a Public Health Alert for frozen mushroom risotto products due to misbranding and an undeclared allergen. The product labeled as porcini mushroom risotto bites may actually contain hot dogs in puff pastry, which contain sesame, a known allergen, that is not declared on the product label. The problem was discovered after the firm, the Fillo Factory of  Northvale, NJ, notified the U.S. Food and Drug Administration (FDA) that it had received a consumer complaint reporting that the hot dogs in puff pastry product had been found in a package labeled as mushroom risotto bites. FDA then notified FSIS about the issue. 

https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-frozen-mushroom-risotto-products-due-misbranding-and
FSIS Issues Public Health Alert For Frozen Mushroom Risotto Products Due To Misbranding And Undeclared Allergens
FSIS Announcement

WASHINGTON, Jan. 5, 2024 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for frozen mushroom risotto products due to misbranding and an undeclared allergen. The product labeled as porcini mushroom risotto bites may actually contain hot dogs in puff pastry, which contain sesame, a known allergen, that is not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with an allergy to sesame are aware that these products should not be consumed. A recall was not requested because the product is no longer available for purchase.

Salmonella Outbreak Linked to RTE Charcuterie Meats from NJ Establishment

CDC is reporting a Salmonella outbreak that has been linked to RTE charcuterie meat products produced by a NJ establishment.   As of January 3, 2024, 24 people infected with the outbreak strain of Salmonella have been reported from 14 states. Of 20 people with information available, 5 have been hospitalized; no deaths have been reported.

Eleven people were interviewed and 6 reported eating RTE charcuterie meats. "One person from Minnesota reported becoming ill in December after eating one 9-oz. tray of the 18-oz. package of “Busseto Foods Charcuterie Sampler Prosciutto, Sweet Sopressata, and Dry Coppa.” On December 27, the Minnesota Department of Agriculture collected and tested a sample of the unopened 9-oz. tray sample from that ill person’s home. Testing identified Salmonella I 4:I:- in that sample, and WGS is being conducted to determine if the Salmonella in these recalled charcuterie samplers is the same as the outbreak strain."

Fratelli Beretta USA, Inc., a Mount Olive, N.J. establishment, is recalling approximately 11,097 pounds of Busseto Foods brand ready-to-eat charcuterie meat products that may be contaminated with Salmonella.   The ready-to-eat (RTE) charcuterie sampler product was produced on October 30, 2023.

Unfortunately, this establishment was responsible for another Salmonella outbreak in August, 2021.  In that event, there were 36 reported cases linked to prepackaged uncured antipasto trays.  The company recalled  approximately 862,000 pounds of uncured antipasto products.

https://www.cdc.gov/salmonella/charcuterie-meats-01-24/index.html
Salmonella Outbreak Linked to Charcuterie Meats
Posted January 5, 2024
Fast Facts
Illnesses: 24
Hospitalizations: 5
Deaths: 0
States: 14
Recall: Yes
Investigation status: Active (first posted on January 5, 2024)

CA Firm Recalls BBQ Sauce for Undeclared Fish Due to Mislabeling

Ventura Foods of Brea, Calif.  is recalling Publix Deli Carolina-Style Mustard BBQ Sauce sold exclusively at Publix Super Markets, Inc., because it contains Traditional Sweet & Spicy BBQ Sauce that may contain a fish (anchovy) allergen that is not declared on the label. 

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ventura-foods-issues-allergy-alert-undeclared-fish-anchovy-allergen-publix-deli-carolina-style
Ventura Foods Issues Allergy Alert on Undeclared Fish (Anchovy) Allergen in Publix Deli Carolina- Style Mustard BBQ Sauce
Summary
Company Announcement Date:  January 08, 2024
FDA Publish Date:  January 09, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Due to Undeclared Fish
Company Name:  Ventura Foods
Brand Name:  Publix Deli
Product Description:  Publix Deli Carolina-Style Mustard BBQ Sauce

NY Firm Recalls Dried Longan Fruit Due to Undeclared Sulfites

HY Success Inc. of Brooklyn, NY is recalling its 5 ounce packages of Fat Choy Kee Dried Longan because they contained undeclared sulfites.  The recall was initiated after routine sampling by Florida Department of Agriculture and Consumer Services and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in the 5 ounce packages of Dried Longan which were not declared on the label. Analysis of the Dried Longan revealed they contained 22.21 milligrams per serving.

Longan fruit (Dimocarpus Longan) is a small and white-fleshed tropical fruit.  This fruit is from the soapberry family, which also includes fruits such as lychee and rambutan. (soruce).

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/hy-success-inc-alert-undeclared-sulfites-fat-choy-kee-dried-longan
HY Success Inc. Alert on Undeclared Sulfites in Fat Choy Kee Dried Longan
Summary
Company Announcement Date:  January 09, 2024
FDA Publish Date:  January 09, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Undeclared sulfites
Company Name:  HY Success, Inc.
Brand Name:  Fat Choy Kee
Product Description:  Dried Longan

NC Firm Recalls Spice Mixes Due to Undeclared Wheat

Vesta Fiery Gourmet Foods, Inc., of Raleigh, NC - JANUARY 8, 2024, is voluntarily recalling various  spice mixes because these products contain undeclared wheat. On 1/4/24 the firm was notified by the North Carolina Depart of Agriculture and Consumer Services that the label does not state the flour used is a wheat flour.  These products were packaged in glass jars and sold primarily online, in retail stores & deli cases located throughout the United States. Images of the products are below.

This would be a label design failure.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vesta-fiery-gourmet-foods-issues-allergy-alert-undeclared-wheat-15oz-glass-jars-benny-ts-vesta-dry
Vesta Fiery Gourmet Foods Issues Allergy Alert on Undeclared Wheat in 1.5oz Glass Jars of Benny T’s Vesta Dry Hot Sauces
Summary
Company Announcement Date:  January 08, 2024
FDA Publish Date:  January 09, 2024
Product Type:  Food & Beverages  Gravy/Sauces
Reason for Announcement:  Due to Undeclared Wheat
Company Name:  Vesta Fiery Gourmet Foods, Inc.
Brand Name:  Benny T’s
Product Description:  Benny T’s Vesta Dry Hot Sauces

Colorado Firm Recalls Parrot Food After FDA Testing Finds Salmonella

D&D Commodities Ltd., Greeley, CO, is voluntarily recalling one lot of 3-D® Pet Products Premium Parrot Food, 4 lb. jar, UPC 719195135045, Lot Number 102525G, due to potential Salmonella contamination.  The recall notification is being issued based on a single manufacturing batch wherein a sample with the Lot Number 102525G and UPC 719195135045 had a positive result for Salmonella in a random sample test collected by the U.S. Food and Drug Administration (FDA) on November 30, 2023. The 3-D® Pet Product Premium Parrot Food was originally manufactured on October 25, 2023.

It will be interesting to see if additional lots are recalled.  This may be hard to limit this recall to one lot without good reason.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/urgent-voluntary-recall-dd-commodities-ltd-3-d-pet-products-premium-parrot-food-due-potential
Urgent Voluntary Recall of D&D Commodities Ltd. 3-D Pet Products Premium Parrot Food Due to Potential Salmonella Contamination
Summary
Company Announcement Date:  January 04, 2024
FDA Publish Date:  January 05, 2024
Product Type:  Animal & Veterinary  Food & Beverages
Reason for Announcement:  Due to potential Salmonella contamination
Company Name:  D&D Commodities, Ltd.
Brand Name:  3-D Pet Products
Product Description:  Parrot Food

Florida Firm Recalls Snack Bars With Undeclared Allergens Due to Improper Label Design

ToYou Snacks, of Winter Garden, Florida is recalling TOYOU branded snack bars in flavors Coconut Mocha, Chocolate Mango, Salted caramel dark chocolate, Mint Dark chocolate, Banana foster, Mango Yogurt because they contain undeclared soy.  "The recall was initiated after it was discovered that the wrappers were missing the soy allergen declaration in the flavors listed above. This issue was caused by mass printing wraps and not having anyone in the team previous to myself [the owner?] and my team with any knowledge on quality and control the company."

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/toyou-snacks-issues-allergy-alert-toyou-snacks-snack-bars-due-undeclared-soy
TOYOU SNACKS Issues Allergy Alert On ToYou Snacks Snack Bars Due to Undeclared Soy
Summary
Company Announcement Date:  January 05, 2024
FDA Publish Date:  January 05, 2024
Product Type:  Food & Beverages
Reason for Announcement:  Due to Undeclared Soy
Company Name:  ToYou Snacks
Brand Name:  ToYou
Product Description:  Snack Bars in a variety of flavors

NJ Firm Recalls Dried Plums Due to Undeclared Sulfites

Win Luck Trading Inc. of Bayonne, NJ, is recalling its "Plum Queen" Dried Plums because they may contain undeclared sulfites.  The recall was initiated after routine sampling by the New York State Department of Agriculture and Markets found sulfites in the product which was distributed in packaging that did not reveal the presence of sulfites. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.  The recalled "Plum Queen" Dried Plums were distributed in New York and New Jersey in retail stores.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/win-luck-trading-inc-issues-allergy-alert-undeclared-sulfites-dried-plums
Win Luck Trading Inc. Issues Allergy Alert on Undeclared Sulfites in Dried Plums
Summary
Company Announcement Date: January 03, 2024
FDA Publish Date:  January 04, 2024
Product Type:  Food & Beverages
Reason for Announcement:  May contain undeclared sulfites
Company Name:  Win Luck Trading, Inc.
Brand Name:  Tasty Snacks
Product Description:  Dried Plums

NC Firm Recalls Additional Lots of Kitten and Puppy Food Due to Salmonella

Blue Ridge Beef is expanding their recall of kitten and puppy foods with potential Salmonella to include additional lot numbers .   The initial was issued on December 21, 2023.  The food is a raw pet food packed in tubes.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/expanded-affected-states-blue-ridge-beef-issues-voluntary-recall-blue-ridge-beef-kitten-grind-blue
Expanded Affected States: Blue Ridge Beef Issues Voluntary Recall of Blue Ridge Beef Kitten Grind, Blue Ridge Kitten Mix and Blue Ridge Beef Puppy Mix Due to Salmonella and Listeria Monocytogenes Contamination
Summary
Company Announcement Date:  December 22, 2023
FDA Publish Date:  January 03, 2024
Product Type:  Animal & Veterinary
Reason for Announcement:  Potential contamination of Salmonella and Listeria monocytogenes
Company Name:  Blue Ridge Beef
Brand Name:  Blue Ridge Beef
Product Description:  Kitten Grind, Kitten Mix, and Puppy Mix

Powdered Infant Formula Recalled for Potential Cronobacter Found by Lab Outside of US

Reckitt/Mead Johnson Nutrition (MJN), a producer of nutrition products, announced today that it has voluntarily chosen to recall from the U.S. market select batches of Nutramigen Powder, a specialty infant formula for the dietary management of Cows Milk Allergy (CMA) in 12.6 and 19.8 oz cans, due to a possibility of contamination with Cronobacter sakazakii in product sampled outside the U.S. All product in question went through extensive testing by MJN and tested negative for the bacteria.

Nutramigen in 12.6 and 19.8 oz containers was manufactured in June 2023 and distributed primarily in June, July, and August 2023. Based on the limited availability of the remaining stock of this special infant formula, it is believed that much, if not all, of the products recalled in the United States have been consumed. There are no reports of illnesses or adverse events to date.

These types of cases come up time to time where sampling and testing occurs outside of US.  Questions arise including whether this non-domestic laboratory has the necessary credentials as well as sampling and testing capabilities.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/reckittmead-johnson-nutrition-voluntarily-recalls-select-batches-nutramigen-hypoallergenic-infant
Reckitt/Mead Johnson Nutrition Voluntarily Recalls Select Batches of Nutramigen Hypoallergenic Infant Formula Powder Because of Possible Health Risk
Summary
Company Announcement Date:  December 30, 2023
FDA Publish Date:  December 31, 2023
Product Type:  Food & Beverages  Infant Formula & Foods
Reason for Announcement:  Potential Cronobacter sakazakii contamination
Company Name:  Reckitt/Mead Johnson Nutrition
Brand Name:  Enfamil
Product Description:  Nutramigen Powder infant formula in 12.6 and 19.8oz cans

MD Firm Recalls Soybean Sprouts After State Lab Sampling Finds Listeria

Nam & Son of MD, Jessup, MD is recalling one-pound bags of soybean sprouts, with the sell-by date of December 14, 2023, because it has the potential to be contaminated with Listeria monocytogenes.  The product has been distributed to retail stores in VA ranging from December 6 -7, 2023.  The recall was initiated after a random sample was collected and analyzed by the state of Virginia, which resulted in confirmation of presence Listeria Monocytogenes in the product. The company has actively started investigating the root cause of the problem.

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nam-son-md-recalls-soybean-sprouts-because-possible-health-risk
Nam & Son of MD Recalls Soybean Sprouts Because of Possible Health Risk
Summary
Company Announcement Date:  December 28, 2023
FDA Publish Date:  December 28, 2023
Product Type:  Food & Beverages
Reason for Announcement:  Potential contamination of Listeria monocytogenes
Company Name:  Nam & Son of MD
Brand Name:  Sam Sung
Product Description:  Soybean Sprouts in 1 lb bags

Illinois Establishment Recalls Ground Beef After Testing Finds E. coli O157:H7

Valley Meats, LLC, a Coal Valley, Ill. establishment, is recalling approximately 6,768 pounds of raw ground beef products that may be contaminated with E. coli O157:H7.  The raw ground beef items were produced on December 22, 2023.  The problem was discovered when the establishment notified FSIS that samples of ground beef products submitted to a third-party laboratory for microbiological analysis tested positive for E. coli O157:H7. There have been no confirmed reports of adverse reactions due to consumption of these products.


https://www.fsis.usda.gov/recalls-alerts/valley-meats-llc-recalls-ground-beef-products-due-possible-e--coli-o157h7
Valley Meats, LLC, Recalls Ground Beef Products Due to Possible E. Coli O157:H7 Contamination
FSIS Announcement

WASHINGTON, Dec. 31, 2023 – Valley Meats, LLC, a Coal Valley, Ill. establishment, is recalling approximately 6,768 pounds of raw ground beef products that may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.