Recalls

According to details published online by the Food and Drug Administration (FDA), the recall was initiated on Feb. 21, 2025, and is ongoing. The firm voluntarily launched the recall after identifying the presence of foreign material, classified as a Class II risk, indicating a low probability of serious health consequences but a potential for temporary or reversible effects. 

The recalled products were distributed to customers in 24 states: Alabama, California, Colorado, Florida, Georgia, Illinois, Indiana, Kansas, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Texas, Virginia, Washington and Wisconsin. 

Recalled Products: 

Market Pantry Soup & Oyster Crackers 

• Item Description: NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case
• UPC: 085239114933
• Code Information: Sell By Date: 23 MAY 2025; Code Date: 23MAY2025BC06
• Product Quantity: 3,330 cases
• Distributed By: Target Corporation, Minneapolis, MN 55403
• Recall Number: F-0622-2025 

Great Value Soup & Oyster Crackers 

• Item Description: NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case
• UPC: 078742085494
• Code Information: Sell By Date: MAY23 2025; Code Dates: MAY 23 2025 ABO6, MAY 23 2025 BBO6, MAY 23 2025 CBO6
• Product Quantity: 9,720 cases
• Distributed By: Walmart, Inc., Bentonville, AR 72716
• Recall Number: F-0622-2025 

Giant Eagle Oyster Crackers 

• Item Description: NET WT 9 OZ (255g), packaged in flexible plastic bags, 12 count per case
• UPC: 030034915087
• Code Information: Best By Date: MAY24 2025; Code Date: MAY 24 25 AB06
• Product Quantity: 990 cases
• Distributed By: Giant Eagle, Inc., Pittsburgh, PA 15238
• Recall Number: F-0622-2025 

VISTA Soup & Oyster Crackers 

• Item Description: NET WT 12 OZ (340g), packaged in flexible plastic bags, 12 count per case
• UPC: 045100008006
• Code Information: Best By Date: MAY24 2025; Code Date: MAY 24 25 AB06
• Product Quantity: 1,440 cases
• Manufactured By: Shearer’s Foods LLC, 100 Lincoln Way East, Massillon, OH 44646
• Recall Number: F-0622-2025 

20lb. Bulk Oyster Crackers 

• Item Description: NET WT 20 LBS., packaged in 20 lb. bulk bag-in-box (not for sale at retail)
• UPC: 10045100400203
• Code Information: Best By: MAY24 2025; Code Dates: MAY 24 25 AB06, MAY 24 25 BB06
• Product Quantity: 394 cases
• Manufactured By: Shearer’s Foods LLC, 100 Lincoln Way East, Massillon, OH 44646
• Recall Number: F-0622-2025 

Retailers and consumers should not use, sell, serve, or distribute the affected products. 

About foreign material contamination 

Stainless steel wire fragments in food pose a risk of injury to the mouth, throat or digestive tract if ingested, as well as a potential choking hazard. Consumers who have consumed the recalled oyster crackers and experience symptoms such as pain, difficulty swallowing or unusual discomfort should seek medical attention promptly. While the Class II classification suggests a low risk of serious adverse health effects, the presence of foreign material remains a safety concern requiring immediate action.

Audience 

• Restaurants and food retailers in California (CA) that have purchased frozen half-shell oysters from KR-7-SP, harvested on 1/30/2024 and 2/4/2024 from Designated Area II in the Republic of Korea (ROK).
• Consumers in CA that have purchased frozen half-shell oysters from KR-7-SP, harvested on 1/30/2024 and 2/4/2024 from Designated Area II in the Republic of Korea (ROK). 

Product 

The implicated product is frozen half shell oysters from KR-7-SP, harvested on 1/30/2024 and 2/4/2024 from Designated Area II in the ROK. The product was recalled by the importer, Sea Win, Inc. (CA 353 SS) of Los Angeles, CA, on 3/7/2025. 

The following photo is included as an example of shellfish labeling that would be attached to containers for reference. 

Purpose 

Sea Win (CA 353 SS) of Los Angeles, CA has recalled frozen half-shell oysters from KR-7-SP, harvested on 1/30/2024 and 2/4/2024 from Designated Area II in the ROK due to an outbreak of norovirus illnesses. The frozen half-shell oysters were distributed in CA and may have been distributed to other states as well. The FDA is advising restaurants and food retailers not to serve or sell and to dispose of, and consumers not to eat, these frozen half-shell oysters because they may be contaminated with norovirus.

Oysters contaminated with norovirus can cause illness if eaten, and potentially severe illness in people with compromised immune systems. Food containing norovirus may look, smell, and taste normal. Consumers of these products who are experiencing symptoms of illness should contact their healthcare provider and report their symptoms to their local Health Department. Diarrhea, abdominal cramps, nausea, vomiting, and fever may be associated with gastroenteritis infections caused by norovirus.

Symptoms of Norovirus 

People of all ages can become infected and get sick with norovirus. The most common symptoms of norovirus are diarrhea, vomiting, nausea, and stomach pain. Other symptoms include fever, headache, and body ache. 

A person usually develops symptoms 12 to 48 hours after being exposed to norovirus. Most people with norovirus illness get better within 1 to 3 days. 

If you have norovirus illness, you can feel extremely ill, and vomit or have diarrhea many times a day. This can lead to dehydration, especially in young children, older adults, and people with other illnesses. Symptoms of dehydration include decrease in urination, dry mouth and throat, and feeling dizzy when standing up. Children who are dehydrated may cry with few or no tears and be unusually sleepy or fussy. 

If you think you or someone you are caring for is severely dehydrated, call your healthcare provider. 

Summary of Problem and Scope 

The California Department of Health notified the FDA of the norovirus outbreak and the 3/7/2025 recall by Sea Win (CA 358 SP) of frozen half shell oysters from KR-7-SP, harvested on 1/30/2024 and 2/4/2024 from Designated Area II in the ROK due to the norovirus outbreak. The frozen half-shell oysters were shipped to distributors and retailers in CA and 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 consumers not to eat frozen half-shell oysters from KR-7-SP, harvested on 1/30/2024 and 2/4/2024 from Designated Area II in the ROK, due to possible norovirus contamination. The oysters were shipped to a distributor in CA and may have been distributed to other states as well. The FDA awaits further information on distribution of these frozen half-shell oysters 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 these potentially contaminated frozen half-shell oysters and restaurants and retailers should dispose of any products by throwing them in the garbage or contacting their distributor to arrange for 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. Their employees 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.
• 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 these potentially contaminated oysters. 

Consumers who have symptoms should contact their health care provider to report their symptoms and receive care. 

For additional assistance, visit Get Assistance from the FDA Human Food Program. 

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Additional Information 

• Notice of Illness Outbreaks, Shellfish Closures, Reopenings, & Recalls - ISSC
• Norovirus | Norovirus | CDC
• About Norovirus | Norovirus | CDC
• How to Prevent Norovirus | Norovirus | CDC
• About Handwashing as a Healthy Habit in the Kitchen | Clean Hands | CDC

The recalled Enoki Mushrooms were distributed to wholesalers in NY that distributed to other states. The recalled product comes in a clear plastic package printed with yellow and green ink declaring Daily Veggies Enoki Mushroom Product of Korea Net Wt. 200g (7.05oz) and marked with UPC code 8809159458890 on the back label. This recall includes all lots. 

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

The contamination was discovered after samples were collected from a store in West Virginia on 1/14/2025 and subsequent analysis by West Virginia Department of Agriculture revealed the presence of Listeria Monocytogenes in some 200g packages of Daily Veggies Enoki Mushroom from Korea. 

Consumers who have purchased 200g packages of Daily Veggies Enoki Mushroom should not consume the products and are urged to destroy the products immediately or return them to the place of purchase for a full refund. Consumers with questions may contact the company at 718-808-1018 between 9am to 2pm Eastern Time, Monday through Friday.

According to details published online by the Food and Drug Administration (FDA), the recall was initiated on Feb. 21, 2025, and remains ongoing. The firm voluntarily launched the recall after receiving reports of spoilage and illness linked to the products, which have been classified as a Class II risk. This classification indicates a low probability of serious health consequences but a potential for temporary or reversible effects. 

The recalled coffee creamers were distributed to retail locations across 31 states: Alabama, Arkansas, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Virginia, Wisconsin and Wyoming. 

Recalled Products: 

Hazelnut International Delight Coffee Creamer 

• Item Description: 32 fl oz (1 qt), 946 mL
• UPC: 0 41271 02565 2
• Code Information: BEST BY: 02 JUL 2025 51-4114 R-S
• Product Quantity: 4,762 cases (6 bottles per case, totaling 28,572 bottles)
• Recall Number: F-0626-2025 

Cinnabon Classic Cinnamon Roll International Delight Coffee Creamer 

• Item Description: 32 fl oz (1 qt), 946 mL
• UPC: 0 41271 01993 3
• Code Information: BEST BY: 03 JUL 2025 51-4114 R-S
• Product Quantity: 7,747 cases (6 bottles per case, totaling 46,482 bottles)
• Recall Number: F-0625-2025 

Retailers and consumers should not use, sell, serve, or distribute the affected products. 

About spoilage and illness concerns 

Spoilage in coffee creamers can result from microbial contamination or product degradation, potentially leading to off-flavors, odors, or textures. The firm received consumer complaints linking the use of these products to illness, though specific symptoms were not detailed in the recall notice. A Class II classification suggests that any adverse effects are likely temporary or reversible, but consumers experiencing unusual symptoms—such as nausea, digestive discomfort, or other reactions—after using these products should seek medical attention promptly.

The lily flowers were distributed to retailers Nationwide.

The lily flowers are individually packed in plastic packaging. Below is the product being recalled:

The recall was initiated after Florida Dept of Agriculture and Consumer Services collected a sample of the lily flowers. It was discovered that lily flowers containing sulfites were distributed in packaging that did not reveal the presence of sulfites.

No illnesses have been reported to date.

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

Customers with a sulfite allergy or sensitivity who have purchased the affected product are urged not to consume the product and dispose of it or return it to their place of purchase for a full refund.

Consumers with questions may contact U.S. Trading Company at 510-781-1818 Monday thru Friday between 8:00am - 4:30pm PST.

Bennett's Sheep Feed (50lb. bag) from Bennett's Feed & Seed in Albany, GA. 
Sheep Mineral Free Choice (50lb. bag), Lot:12/06/2023, from W.B. Fleming in Tifton, GA.

Please be aware that the Stop Sale only applies to Lot:12/06/2023 and Bennett's Sheep Feed which is a custom feed. Please avoid feeding these items to sheep to ensure their safety. For more information, please contact our office at (404) 656-4958.  

The Glicks Dark Chocolate Conettos were distributed to stores nationwide, predominately located in the New York, New Jersey and Connecticut regions, during the weeks of October 13th, 2024 through February 14th, 2025. Some units were sold on Amazon.com.

This recall was initiated after the company was notified by their Quality Control Department that a limited number of bags labeled as “Dark Chocolate Conettos” contained Milk Chocolate Conettos, which contains milk allergen that is not declared on the label.

Only packages bearing the Lot Code below, may potentially have milk Conettos in the “darkchocolate Conettos” bag.

The company has received no reports of illness or injury to date.

We immediately informed all retailers who had purchased this lot code about this recall and instructed them to inspect their inventory or remove any potential affected product on their shelves.

Consumers who may have purchased this product are advised to inspect their product for the affected Lot Code 02092024. Consumers may return the product for credit or refund. If a consumer experiences an allergic reaction they are urged to report to a medical provider.

Consumers who have questions may contact us at Customercare@kayco.com or by phone at 718-369-4600 Monday through Friday 9 AM to 5PM Eastern Time.

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

Products were distributed through retail stores in Ontario, Canada and the following US states AL, AR, CA, CT, CO, DC, DE, FL, GA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NE, NC, NH, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, VA, WA, WI and WV.

This mislabeling was discovered following receipt of a single consumer complaint involving an allergic reaction. The issue originated from a supplier who inadvertently failed to fully disclose all allergens while translating the ingredient list. We are actively working with the supplier to implement stricter labeling controls, including an additional verification process for multilingual labels.

Consumers who have purchased any of the below Ulker Brand products are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at info@ziyad.com.

See Product List

The impacted products were distributed to retail stores as follows:

• H-E-B label - Texas
• Trader Joe’s label – Delaware, Illinois, Indiana, Iowa, Kansas, Kentucky, Maryland, Michigan, Minnesota, Missouri, Nebraska, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Virginia, Washington D.C., and Wisconsin
• Genova 7 oz. - Costco in Florida and Georgia
• Genova 5 oz. - Harris Teeter, Publix, H-E-B, Kroger, Safeway, Walmart, and independent retailers in Alabama, Arkansas, Arizona, California, Florida, Georgia, North Carolina, New Jersey, Tennessee, and Texas
• Van Camp’s label – Walmart and independent retailers in Pennsylvania, Florida and New Jersey

Recalled products include specific can codes and Best if Used By dates indicated on the bottom of the cans, and UPC numbers listed below.

If you have a recalled tuna can, please return it to the retailer for a full refund, throw it away, or contact Tri-Union Seafoods directly for a retrieval kit and a coupon for a replacement product. Consumers can contact Tri-Union Seafoods at support@thaiunionhelp.zendesk.com or 833-374-0171, if they have any questions or to request replacement product. The toll-free number hours are Monday through Friday from 9:00 a.m. to 5:00 p.m. EST.

This recall does not impact any other Tri-Union Seafoods products, as no other product packaging was impacted by this potential defect. Tri-Union Seafoods is committed to upholding the highest safety and quality standards.

For media inquiries, contact Media.Inquiries@thaiunion.com.

Tri-Union Seafoods advises that consumers in possession of any product with the below Lot Codes should dispose of the product. Below is a list of specific Lots impacted:

GERBER® SOOTHE N CHEW® TEETHING STICKS were distributed nationwide via the internet and to distribution centers and retail stores in the following states and territories: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI and Puerto Rico.

Recalled products can be identified as follows:

• GERBER® SOOTHE N CHEW® TEETHING STICKS – STRAWBERRY APPLE, Net Wt. 3.2 Oz (90g), with UPC 0 15000 04618 7, all lot codes
• GERBER® SOOTHE N CHEW® TEETHING STICKS – BANANA, Net Wt. 3.2 Oz (90g), with UPC 0 15000 04608 8, all lot codes
• GERBER® SOOTHE N CHEW® TEETHING STICKS – BANANA, Net Wt. 1.59 Oz (45g), with UPC 0 15000 01015 7, all lot codes

This recall and discontinuation is isolated to GERBER® SOOTHE N CHEW® TEETHING STICKS – STRAWBERRY APPLE and GERBER® SOOTHE N CHEW® TEETHING STICKS – BANANA.

The recall was initiated after receiving consumer complaints of choking incidents. To date, one emergency room visit has been reported to the firm.

Consumers who may have purchased GERBER® SOOTHE N CHEW® TEETHING STICKS should not feed this product to their child and can return the product to the retailer where it was purchased for a refund. Anyone concerned about an injury or illness should contact a health care provider. For any additional support needed, Gerber is available 24/7 at 1-800-4-GERBER (1-800-443-7237).

We are working with the U.S. Food & Drug Administration (FDA) on this recall and will cooperate with them fully.

We sincerely apologize for any concern or inconvenience this action represents to parents, caregivers and retail customers.

(Press Release URL: https://www.nestleusa.com/media/pressreleases/gerber-recalldiscontinuation-soothe-n-chew-teething-sticks)