Recalls

The ready-to-eat liverwurst products were produced between June 11, 2024, and July 17, 2024, and have a 44-day shelf life. The following liverwurst products are subject to recall [view labels]:       

• 3.5-lb. loaves in plastic casing, or various weight packages sliced in retail delis, containing “Boar’s Head Strassburger Brand Liverwurst MADE IN VIRGINIA.” The products shipped to retailers bear sell by dates ranging July 25, 2024, to Aug. 30, 2024, printed on the side of the packaging.

The other ready-to-eat deli meat products were produced on June 27, 2024. The following deli meat products are subject to recall:

• 9.5-lb. and 4.5-lb. full product, or various weight packages sliced in retail delis, containing “Boar’s Head VIRGINIA HAM OLD FASHIONED HAM” with sell by date “AUG 10” on the product packaging.
• 4-lb., or various weight packages sliced in retail delis, containing “Boar’s Head ITALIAN CAPPY STYLE HAM” with sell by date “AUG 10” on the product packaging.
• 6-lb., or various weight packages sliced in retail delis, containing “Boar’s Head EXTRA HOT ITALIAN CAPPY STYLE HAM” with sell by date “AUG 10” on the product packaging.
• 4-lb., or various weight packages sliced in retail delis, containing “Boar’s Head BOLOGNA” with sell by date “AUG 10” on the product packaging.
• 2.5-lb., or various weight packages sliced in retail delis, containing “Boar’s Head BEEF SALAMI” with sell by date “AUG 10” on the product packaging.
• 5.5-lb., or various weight packages sliced in retail delis, containing “Boar’s Head STEAKHOUSE ROASTED BACON HEAT & EAT” with sell by date “AUG 15” on the product packaging.
• 3-lb., or various weight packages sliced in retail delis, containing “Boar’s Head GARLIC BOLOGNA” with sell by date “AUG 10” on the product packaging.
• 3-lb., or various weight packages sliced in retail delis, containing “Boar’s Head BEEF BOLOGNA” with sell by date “AUG 10” on the product packaging.                                   

The products subject to recall were distributed to retail deli locations nationwide. The products shipped to deli retailers bear establishment number “EST. 12612” inside the USDA mark of inspection on the product labels.

The problem was discovered when FSIS was notified that a sample collected by the Maryland Department of Health tested positive for L. monocytogenes. The Maryland Department of Health, in collaboration with the Baltimore City Health Department, collected an unopened liverwurst product from a retail store for testing as part of an outbreak investigation of L. monocytogenes infections. Further testing is ongoing to determine if the product sample is related to the outbreak. Anyone concerned about illness should contact a healthcare provider. 

FSIS is working with the Centers for Disease Control and Prevention (CDC) and state public health partners to investigate the multistate outbreak of L. monocytogenes infections linked to meats sliced at delis. As of July 25, 2024, 34 sick people have been identified in 13 states, including 33 hospitalizations and two deaths. Samples were collected from sick people from May 29, 2024, to July 12, 2024. Additional information may be found on the CDC investigation notice, Listeria Outbreak Linked to Meats Sliced at Delis. The investigation is ongoing, and FSIS continues to work with the CDC and state partners.

Consumers with questions regarding the recall can contact Boar’s Head Provisions Co., Inc., Customer Service at 1-800-352-6277. Media with questions can contact Elizabeth Ward, Vice President of Communications, Boar’s Head Provisions Co., Inc., at media@boarshead.com.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

The cheese has been distributed in two sizes, an 8-ounce wedge in a clear plastic package, and a full 15-pound wheel in a clear plastic package, marked with a logo sticker with ingredients listed on the top and with the lot number 231129 on a white label on the side.

No illnesses have been reported to date in connection with this recalled lot.

The potential for contamination was noted after routine testing by the Kentucky Department of Public Health revealed the presence of Listeria monocytogenes in a package of St. Jerome batch 231129.
The production of the product has been suspended while the FDA and the company continue to investigate the source of the problem.

Consumers who have purchased should not consume the product and are urged to return them to the place of purchase for a full refund or dispose of the product. Consumers with questions may contact the company at 1-270-434-4124 or email kenny@kennyscheese.com from Monday through Friday, 8:00AM-4:00PM.

The recalled Al’Fez Natural Tahini was distributed nationwide in retail stores beginning 05/26/23. The recalled Al’Fez Natural Tahini was sold in 5.6oz glass jars, UPC 711464506778, and with a “BEST BEFORE” of “2024 JL 11” or later. The specific codes being recalled are: Lot Numbers “3031”, “3080”, “3270”, “3297” with corresponding BEST BEFORE: “2024 JL 31”; “2024 SE 09”; “2025 MR 27”; “2025 AL 04”. The recall only applies to these codes, the codes are located on the back of the jar as depicted in the pictures below.

To date, AB World Foods US, Inc. has received no reports of illness related to the recalled product from consumers in the United States.

The potential for contamination was noted after testing by the company revealed the presence of Salmonella. The company has ceased distribution of the product as the company continues their investigation.

Consumers who have purchased Al’Fez Natural Tahini 5.6oz with the affected lot codes are advised to discontinue use immediately and return the product to the place of purchase for a full refund. If a consumer experiences the symptoms listed above and believes they may have been exposed to Salmonella, they are urged to contact a medical provider.

The wellbeing of its customers is paramount to AB World Foods US, Inc. Consumers who have questions may contact Adifi Burman, info@alfez.us, 647 218 0081. Monday through Friday 9 a.m. to 5 p.m. Eastern Time.

This recall is being made with the knowledge of the Food and Drug Administration.

The recalled "ALDI - Bakeshop Chocolate Chip Muffin 4 count" were distributed nationwide in ALDI retail stores.

The recalled "ALDI - Bakeshop Chocolate Chip Muffin 4 count" comes in a clear plastic clamshell containing 4 muffins and has a red label. The recalled Bakeshop Chocolate Chip Muffin 4 count are marked with lot # NF1 142Y on the top and UPC on the label 4099100048278. 

No illnesses or adverse effects have been reported to date in connection with this problem.

The recall was initiated after it was discovered that the walnut-containing product was distributed in packaging that did not reveal the presence of walnut. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.

Production of the product has been suspended until the FDA and the company are certain that the problem has been corrected.

Consumers who have purchased 4 count packages of "ALDI - Bakeshop Chocolate Chip Muffin" are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at customercare@fgfbrands.com.

Product Details

Product Name: Foppen Smoked Norwegian Salmon Slices – Toast sized
UPC code: 8 40137 10000 2
Package Size: 8.1 oz

LOT 412 – to be found in the clear plastic window cut out on the front of the package.

Distribution: Kroger and Payless Supermarkets. The states involved are AL, AR, GA, IL, IN, KY, LA, MI, MO, MS, OH, SC, TN, TX and WV.

Consumer Actions

Consumers should discard product or return for refund. Customers who have purchased the affected Smoked Norwegian Salmon Slices with lot number 412 are advised not to consume the product. They should return it to the place of purchase for a full refund or replacement. For any questions or concerns, consumers may contact Foppen Seafood office USA at US PHONE NUMBER of 844-646-0928 (24/7) or mail supportQ1087@foppenseafood.com.

Company Statement

“At Foppen Seafood, we operate to the highest standards of health, safety and quality control. We have taken immediate steps to address this isolated incident and we are collaborating closely with Kroger and the U.S. Food and Drug Administration (FDA) to ensure a swift resolution.”

Health Information

Consumers who have consumed the affected product and are experiencing symptoms such as fever, muscle aches, and gastrointestinal issues should seek medical attention. For more information about Listeria monocytogenes, consumers can visit the Centers for Disease Control and Prevention (CDC) website.

For media requests mail supportQ1087@foppenseafood.com.

For updates on this recall and other important information, please visit Foppen Seafood’s official website at https://www.foppenseafood.com

Products were distributed nationwide, and available in retail locations and direct delivery.

The products included in the recall is linked in the list below. 

Product can be identified by comparing the date and plant information on the product. Example photographs of the impacted product are provided below.

No illnesses have been reported to date.

Totally Cool, Inc. has ceased the production and distribution of the affected products due to FDA sampling which discovered the presence of Listeria monocytogenes. The company continues its investigation and is taking preventive actions. No other products produced by Totally Cool, Inc. are impacted by this recall.

Consumers who have recalled product in their possession are urged to return it to the place of purchase for a full refund. Consumers with questions may contact Totally Cool, Inc. at 410-363- 7801 and regulatory@totallycoolicecream.com, between 8am and 4pm eastern, Monday to Friday.

Link to Product Table and Images

The products were distributed nationwide through various coffee roasters and retail locations, as well as through direct online purchase from Snapchill. The problem was identified when the U.S. Food and Drug Administration (FDA) notified Snapchill that the low acid canned foods process for manufacturing the recalled products was not filed with FDA, as is required by regulation. No illnesses have been reported to-date, and Snapchill is not aware of any instances in which the company’s products contained botulin toxin. Snapchill is working on filing the appropriate notification with FDA.

The products are sold under a range of roaster and brand names, in variety of metal can sizes ranging from 7 oz to 12 oz. The products are identifiable by the language “Produced and distributed by Snapchill LLC” underneath the nutrition facts panel. Some of the products can also be identified by the text “Snapchill Coffee” on the label. The specific products subject to this voluntary recall are listed at the end of this notice.

This voluntary recall is being made with the knowledge of FDA.

Consumers should either destroy the products or return the product to Snapchill or the place of purchase for a refund. Snapchill will offer full refunds for any of these products, with appropriate proof of purchase including a picture of the product(s) before being destroyed. Full information about the return and refund will be available at Compliance@Snapchill.com.

Consumers with questions may contact the company any time by email at Compliance@snapchill.com, or by phone, Monday through Friday between 8:00am and 4:00pm Central Time, at (920) 632-6018.

The specific products subject to this voluntary recall are as follows (listed in alphabetical order):

Product List

Aahu Barah Apricot Roll 14OZ was distributed in New York, Texas, Virginia, Maryland, Pennsylvania and Georgia through retail stores.

The product is sold in clear plastic bags [6 inch by 8 inch] packing with the Aahu Barah Label on the front and back. The product is labeled Apricot Roll on both the front and back. The size of the product is 14 OZ, the expiration date is Dec 2025, the UPC code is 882475000279.

No illnesses or allergic reactions involving this product have been reported to date.

The undeclared sulfites was discovered after sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of Sulfites in the Apricot Roll.

Consumers who have purchased Aahu Barah Apricot Roll 14 OZ are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 516-396-0710.

• Restaurants and food retailers in California (CA) that have recently purchased oysters from Dailyfresh Shellfish, Inc., with lot # 240531JM harvested from Subarea 23-10 in British Columbia (BC), Canada on 5/30/2024.
• Consumers in CA that have recently purchased oysters from Dailyfresh Shellfish, Inc., with lot # 240531JM harvested from Subarea 23-10 in BC, Canada on 5/30/2024.

Product

Dailyfresh Shellfish, Inc., live Pacific oysters, with lot # 240531JM harvested from Subarea 23-10 in BC, Canada on 5/30/2024. The oysters were distributed to restaurants and retailers in CA and may have been distributed to other states as well.

Purpose

The FDA is advising restaurants and food retailers not to serve or sell and to dispose of, and consumers not to eat, oysters from Dailyfresh Shellfish, Inc., with lot # 240531JM harvested from Subarea 23-10 in British Columbia (BC), Canada on 5/30/2024 because they may be contaminated with the toxins that cause paralytic shellfish poisoning (PSP).

Molluscan shellfish contaminated with natural toxins from the water in which they lived can cause consumer illness. Most of these toxins are produced by naturally occurring marine algae (phytoplankton). Molluscan shellfish consume the algae which causes the toxins to accumulate in the shellfish’s flesh. Typically, contamination occurs following blooms of the toxic algal species; however, toxin contamination is possible even when algal concentrations are low in certain instances. One of the recognized natural toxin poisoning syndromes that can occur from consuming contaminated molluscan shellfish is paralytic shellfish poisoning (PSP).

PSP is caused by neurotoxins also referred to as saxitoxins or paralytic shellfish toxins (PSTs). Shellfish can retain the toxin for different lengths of time. Some species cleanse themselves of toxins rapidly, whereas others are much slower to remove the toxins. This lengthens the period of time they pose a human health risk from consumption.

Food containing PSTs may look, smell, and taste normal. These toxins cannot be removed by cooking or freezing. Consumers of these products who are experiencing symptoms of illness should contact their healthcare provider and report their symptoms to their local Health Department.

Symptoms of Paralytic Shellfish Poisoning

Most people with PSP will begin to develop symptoms within 30 minutes of consuming contaminated seafood. Effects of PSP intoxication can range from tingling of the lips, mouth, and tongue to respiratory paralysis and may include these other symptoms: numbness of arms and legs, “pins and needles” sensation, weakness, loss of muscle coordination, floating feeling, nausea, shortness of breath, dizziness, vomiting, and headache. Medical treatment consists of providing respiratory support and fluid therapy. For patients surviving 24 hours, with or without respiratory support, the prognosis is considered good, with no lasting side effects. In fatal cases, death is typically due to asphyxiation. 

Due to the range in severity of illness, people should consult their healthcare provider if they suspect that they have developed symptoms that resemble paralytic shellfish poisoning.

Summary of Problem and Scope

On 6/10/2024 the Canadian Food Inspection Agency (CFIA) advised the FDA that recent monitoring detected elevated levels of paralytic shellfish toxins in shellfish harvested from Subarea 23-10 in British Columbia, Canada. CFIA advised the FDA that live oysters from Dailyfresh Shellfish, Inc., with Lot # 240531JM were harvested from Subarea 23-10 in BC, Canada on 05/30/2024 and had been shipped to distributors in California. The product may have been distributed to other states as well.

FDA Actions

The FDA is issuing this alert advising restaurants and food retailers not to serve or sell and advising consumers not to eat Dailyfresh Shellfish, Inc. oysters with Lot #240531JM harvested from Subarea 23-10 in BC, Canada on 5/30/2024 due to possible contamination with paralytic shellfish toxins. 

The FDA is awaiting further information on distribution of the shellfish harvested and will continue to monitor the investigation and provide assistance to state authorities as needed. As new information becomes available, the FDA will update the safety alert.

Recommendations for Restaurants and Retailers

Restaurants and retailers should not serve or sell the potentially contaminated shellfish. Restaurants and retailers should dispose of any products by throwing them in the garbage or contacting their distributor for return and destruction.

Restaurants and retailers should also be aware that shellfish may be a source of pathogens and should control the potential for cross-contamination of food processing equipment and the food processing environment. They should follow the steps below:

• Wash hands with warm water and soap following the cleaning and sanitation process.
• Retailers, restaurants, and other food service operators who have processed and packaged any potentially contaminated products need to be concerned about cross-contamination of cutting surfaces and utensils through contact with the potentially contaminated products and should clean and sanitize food contact surfaces and utensils.
• Retailers that have sold bulk product should clean and sanitize the containers used to hold the product.
• Regular frequent cleaning and sanitizing of food contact surfaces and utensils used in food preparation may help to minimize the likelihood of cross-contamination.

Recommendations for consumers

Consumers should not eat the potentially contaminated shellfish. Consumers who have symptoms of paralytic shellfish poisoning should contact their health care provider to report their symptoms and receive care.

To report a complaint or adverse event (illness or serious allergic reaction), you can:

• Call an FDA Consumer Complaint Coordinator if you wish to speak directly to a person about your problem.
• Complete an electronic Voluntary MedWatch form online.
• Complete a paper Voluntary MedWatch form that can be mailed to FDA.

Visit www.fda.gov/fcic  for additional consumer and industry assistance. 

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Additional Information

• Notice of Illness Outbreaks, Shellfish Closures, Reopenings, & Recalls - ISSC
• Food Poisoning from Marine Toxins | CDC Yellow Book 2024
• Fish and Fishery Products Hazards and Controls
• FDA Bad Bug Book (2nd Edition)
• Handwashing: A Healthy Habit in the Kitchen