Recalls

PH-controlled food products that are not manufactured in accordance with applicable regulatory requirements may present a potential risk of microbial growth, including organisms that can produce toxins associated with botulism. Botulism is a rare but serious illness that can affect the nervous system. Symptoms may include general weakness, dizziness, double vision, difficulty speaking or swallowing, and, in severe cases, difficulty breathing or muscle weakness.

No illnesses or adverse health events have been reported in connection with the products subject to this recall to date.

The affected products were distributed nationwide through select retail, online via truеsеamоss.cоm and other distribution channels.

Recalled product includes all flavors and sizes and batch numbers of True Sea Moss brand Sea Moss Gel Superfood packaged in 16 FL OZ (473 mL) glass jars, manufactured prior to January 9, 2026. The manufacture date (MFD) is indicated on the can lid. Format is MM/YYYY:

Recalled flavors include the following:

The matter was identified during a California Department of Public Health inspection that raised questions regarding regulatory authorization and related production records for certain distributed products. The Company is cooperating fully with regulatory authorities and has initiated this voluntary recall to ensure regulatory alignment.

Consumers who have purchased the affected Sea Moss Gel Superfood products should discontinue use of the product and follow the instructions provided by the place of purchase regarding product return or disposal. Consumers seeking additional information may contact: Email: support@divafam.com Phone: (818) 751-3882, Monday through Friday, 9:00 a.m. – 5:00 p.m. Pacific Time (PT).

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Media Contact: Diva Fam Team
support@divafam.com

No illnesses have been reported to date. That said, customers who have symptoms of listeria infection should contact their healthcare provider.

The affected products were distributed to retail stores and distributors nationwide between November 3, 2025 and November 20, 2025 and include: 

No other Ambriola, Locatelli, Member’s Mark, Pinna, or Boar’s Head products are included in the recall.

Customers who purchased the affected products should not consume them and either dispose of them or return them to the place of purchase for a full refund. For more information, contact Ambriola at 1-800-962-8224 from Monday through Friday from 9:00am – 4:00 pm ET.

“We take food safety very seriously and immediately alerted stores and distributors to remove the affected products from shelves,” said Phil Marfuggi, chief executive officer. “We are working closely with the FDA and continuing to test our products and facilities to fully understand the situation.”

Ambriola has suspended production and distribution of affected products as the Company conducts a thorough review of all sanitation and food safety procedures.

Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly individuals, and others with weakened immune systems. Healthy individuals infected with Salmonella may experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare cases, infection can result in the organism entering the bloodstream and causing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis, and arthritis. Individuals experiencing these symptoms should seek medical attention immediately.

The affected products were available for purchase online and through select retail partners nationwide since September 15, 2025. The recalled products can be identified by brand name (Spring & Mulberry), with the following identifiers: flavor name, lot codes, and box color. The lot code is listed on the back of the packaging and inner flow wrap. Please see an example of the packaging and lot code at the end of the release.

There have been no confirmed illnesses or adverse health effects reported to date. The potential for contamination was first noted after routine third-party testing conducted by the company’s contract manufacturer revealed finished product tested positive for Salmonella.

Because Salmonella can be difficult to detect and may appear intermittently, we are now expanding the recall beyond Mint Leaf in consultation with the FDA to include additional production lots made during the same time period on the same equipment. All other lot codes are unaffected by this recall.

Customers who have purchased the affected product are asked to dispose of it. They may request a refund by contacting Spring & Mulberry at recalls@springandmulberry.com with a photo of the lot code.

We appreciate your cooperation.

For more information or assistance, please contact:

Spring & Mulberry Customer Service
recalls@springandmulberry.com

The RTE holiday kielbasa was produced on Oct. 14, 2025. The following product is subject to recall [view labels]:

• 16-oz. vacuum-sealed plastic packages containing one, fully cooked “OLYMPIA PROVISIONS UNCURED HOLIDAY KIELBASA” with “BEST IF USED BY” date “02/19/26” printed on the side of the label.

The product subject to recall bears establishment number “EST. 39928” inside the USDA mark of inspection. This item was shipped to retail locations in California, Oregon, and Washington, and was available nationwide through online direct-to-consumer sales.                      

The problem was discovered after the establishment notified FSIS that it received a consumer complaint regarding metal found in the product. There have been no confirmed reports of injury due to consumption of this product. Anyone concerned about an injury should contact a healthcare provider.

FSIS is concerned that some product may be in consumer refrigerators or freezers. Consumers who have purchased this product are urged not to consume it. This product should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers and members of the media with questions about the recall can contact Michelle Cairo, Owner, Olympia Provisions at michelle@olympiaprovisions.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 Lorraine Quiche items were produced on April 9, 2025, and April 17, 2025. The following products are subject to recall [view labels]:

• 19.8-lb. cardboard boxes containing “Lorraine Quiche (with pork) La Madeleine” in metal trays wrapped in plastic.

The products subject to recall do not bear a USDA mark of inspection. The affected products bear expiration dates of April 8, 2028, and April 16, 2028. The affected products were shipped to distributors in Georgia, Louisiana, Maryland, North Carolina, and Texas.

The problem was discovered during routine FSIS import surveillance activities. There have been no confirmed reports of illness due to consumption of these products. Anyone concerned about an illness or injury should contact a healthcare provider.  

FSIS is concerned that some product may be in consumer refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify theircustomers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers and members of the media with questions about the recall can contact Ms. Marie-Claude Boucher, Director of Quality Assurance, St-Hubert Group at mboucher@st-hubert.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/.

Choceur branded Cookie Butter Holiday Bark may contain undeclared pecans. People who have allergies to pecans run the risk of serious or life-threatening allergic reaction if they consume these products.

Choceur branded Pecan, Cranberry & Cinnamon Holiday Bark may contain undeclared wheat. People who have allergies to wheat run the risk of serious or life-threatening allergic reaction if they consume these products.

The recalled items were distributed nationwide through Aldi grocery stores.

This expansion includes additional lot numbers and “best by” dates not covered in the original recall.

Cookie Butter Holiday Bark is packed in 5 oz. Choceur branded stand up pouch bags:

• Lot #: 28525 – Best By 05/2026
• Lot #: 29925 – Best By 05/2026
• Lot #: 30625 – Best By 06/2026

Pecan, Cranberry & Cinnamon Holiday Bark is packed in 5 oz. Choceur branded stand up pouch bags:

• Lot #: 28525 – Best By 08/2026
• Lot #: 29925 – Best By 08/2026
• Lot #: 30625 – Best By 09/2026

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

The expanded recall was initiated after it was discovered that the Pecan, Cranberry & Cinnamon Holiday Bark had been packaged in Cookie Butter Holiday Bark packages resulting in undeclared pecan. Subsequent investigation indicates the problem may have been caused by a temporary breakdown in the company’s production and packaging process.

Consumers who have purchased the recalled products are urged to discard the product.

Consumers with questions may contact Silvestri Sweets at 1-630-232-2500 – M-F 8:30am – 4:30pm CST or via email at customerservice@carousel-candies.com.

Link to Initial Press Release

This voluntary recall was initiated on December 15, 2025. The FDA has been informed of this voluntary recall and So Delicious Dairy Free® is working swiftly with retail partners to remove the potentially impacted product from shelves. In the meantime, the company has already identified and corrected this issue and will soon be able to bring back the frozen dessert so many people enjoy.

So Delicious Dairy Free® takes every consumer experience seriously and is initiating this voluntary recall in line with its commitment to product quality and consumer safety.

Consumers who have purchased the affected product should not consume it. For information on refunds, please contact the So Delicious Dairy Free® Care Line at 1-833-367-8975. Consumer Care specialists are available to speak live during business hours (Monday – Friday; 9am – 6pm EST). 

Consumers may also reach out to the Consumer Care team via webform at https://sodeliciousdairyfree.com/contact-us/. 

Packages / containers will appear as below. Packaging graphics for this product changed in February 2025 (no change to UPC).

• 18-lb. cases containing four units of “FULLY COOKED BREADED CHICKEN PORTIONS,” with case code “P-1380 126237 B30851 23:11 K04” printed on the side of the packaging.

The product subject to recall bears the USDA mark of inspection on the case’s label and establishment number “P-1380” printed on the side of the package. These items were shipped to restaurant locations nationwide.

The problem was discovered when the company notified FSIS that they had identified chicken product containing soy that had been mislabeled with a non-allergen containing product code.

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.

FSIS is concerned that some product may be in restaurant refrigerators or freezers. Restaurants are urged not to serve this product; these items should be thrown away.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers with questions about the recall may contact Dawn Duncan, Customer Service Director, Suzanna’s Kitchen at dduncan@suzannaskitchen.com. Members of the media may contact Craig Pate, Chief Financial Officer, Suzanna’s Kitchen at cpate@suzannaskitchen.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 recalled product was shipped to retailers between August and October 2025. The 4-count Original Slider cartons impacted by the recall were sold primarily in convenience stores in potentially all 50 states.

The recalled 4-count, White Castle brand Original Sliders, are packaged in a blue and white cardboard box with UPC# 0-82988-02969-3. Each 4-count carton includes individually wrapped packs of two Sliders.

The recalled lot codes are 9H203521 and 9H203522, which can be found printed within a light-blue bar on the end panel of the carton followed by the best by date.

Please note that only the full lot codes listed above are included in the recall. Any product that does not include all eight characters of the lot codes listed above is not included in the recall.

The cartons of 4-count Original Sliders have a 270-day frozen shelf with Best By Date: April 18, 2026.

During the packaging process, Jalapeño Cheese Sliders were put in the wrong package, and milk and soy are not listed as ingredients or allergens on the packaging. The issue was discovered when a customer notified White Castle that they suffered a non-life-threatening allergic reaction after consuming one of the Jalapeño Cheese Sliders that was incorrectly packaged in the 4-count Original Sliders carton. No other reports of injury or illness have been received to date.

Consumers who purchased the product being recalled are asked to return it to the place of purchase for a full refund. Anyone with questions can contact White Castle at 1-800-843-2728 (24 hours, Sunday-Saturday).

The frozen, retail 4-count cartons of Original Sliders being recalled are packed in the retail cartons shown in the images below.

The recalled Bengal King Jhal Chanachur were distributed nationwide in retail stores and through mail orders. The product comes in a 12.34 oz (350gm), clear plastic jar marked with lot B No.HCNCU1205/24 on the top and with an expiration date of June-2026 stamped on the side. The product UPC code is 8941153046243.

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

The recall was initiated after routine sampling by New York State Department of Agriculture and Markets Food Inspectors and subsequent analysis by Food Laboratory personnel revealed that the peanut-containing product was distributed in packages that did not reveal the presence of peanuts.

Consumers who have purchased 12.34 oz (350gm) packages of Bengal King Jhal Chanachur are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-718-894-2507.