glass Recalls

160 recalls tagged with “glass”.

Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Recalls 307 Cases of Cut Fresh Fruit Mix Over Listeria Risk (2025)

Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Mix due to potential Listeria monocytogenes contamination. The product was packed by WPS in Minneapolis, MN and distributed to five Midwest states. Consumers should not eat the recalled fruit and should contact the distributor for refund or replacement.

Wholesale Produce Supply LLC
Potential Listeria
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Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Recalls 307 Cases of Cut Fresh Fruit Mix Over Listeria Risk (2025)

Wholesale Produce Supply LLC recalled 307 cases of Cut Fresh Fruit Mix after potential Listeria monocytogenes contamination was identified. Affected lots include Fruit Mix HC 6/6 oz, Fruit Medley F&F 4/12 oz, and Fruit Mix Harvest Cuts 4/16 oz Net Wt 1 lb, distributed to IA, IL, ND, NE and WI. Consumers should not eat this product and should contact Wholesale Produce Supply LLC DBA for refund or a

Wholesale Produce Supply LLC
Potential Listeria
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Food & Beverages
HIGH
FDA FOOD

Albertsons Store-Made Grilled Chicken & Basil Pasta Extra Large Recalled for Listeria (2025)

Albertsons Companies is recalling store-made Grilled Chicken & Basil Pasta Extra Large sold under Carrs-Safeway, Eagle and Safeway banners. The product contains a bowtie pasta ingredient recalled for Listeria monocytogenes contamination. It was distributed in AK, AR, AZ, CA, CO, HI, LA, NE, NM, NV, OK, SD, TX, UT and WY. Stop using the product and contact Albertsons for refund or replacement.

Albertsons
Listeria monocytogenes.
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Food & Beverages
HIGH
FDA FOOD

Orwashers Soho Sourdough XL Batard Recalled for Undeclared Sesame Seeds

Orwashers brand Soho Sourdough XL Batard is being recalled after labeling errors could hide sesame seeds. The recall covers 4 pallets of 6 pieces per case in Massachusetts. Consumers should avoid consumption and contact Oven Artisans LLC for refunds or replacements.

Orwashers
Mislabeled: Product
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Health & Personal Care
HIGH
FDA DEVICE

BD Recalls 62 BD MAX System IVD Units Worldwide Over Credential Breach (2025)

BD MAX System recall affects 62 units distributed worldwide in 2025 after unauthorized access to service credentials. An unauthorized actor accessed credentials used by BD technical support teams. Healthcare providers should stop using the devices and follow the manufacturer’s recall instructions.

BD
Product service
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Health & Personal Care
HIGH
FDA DEVICE

BD BACTEC Blood Culture System Recall 1,086 Units Worldwide Over Unauthorized Access Risk (2025)

BD recalled 1,086 BD BACTEC Blood Culture System units worldwide after unauthorized access to product service credentials. The breach could compromise confidentiality, integrity and availability of affected devices and data. Hospitals and healthcare providers should stop using the device immediately and follow BD’s recall instructions.

BD
Product service
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet Bulk Empire Mix Recall for undeclared tree-nut Allergens

Taproom Gourmet bulk Empire Mix recall affects 3,547 cases distributed across New York, New Jersey, Connecticut, California, Illinois and Florida. The product lacks an ingredient label and contains undeclared allergens. Consumers should not consume the product and should seek a refund or replacement from Egress Capital Partners.

Taproom Gourmet
No ingredient
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems LOGIQ P9 R4.5 Ultrasound System Recalled for Inaccurate Liver Readings (37 Units)

GE Medical Systems recalled 37 LOGIQ P9 R4.5 ultrasound systems sold nationwide in the United States and globally after regulators flagged UGAP measurements that may misrepresent liver steatosis. The UGAP data may display inaccurate values representing liver steatosis, potentially guiding inappropriate clinical decisions. Clinicians should stop using the affected devices and await recall guidance.

GE Medical Systems
The Ultrasound-Guided
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Food & Beverages
HIGH
FDA FOOD

Goyal Group SILVER HORSE Aluminum Milk Pan & Mathar Kadaï Recalled for Lead Contamination (293 Sets,

Goyal Group Inc. recalled 293 sets of SILVER HORSE aluminum cookware, including a 4-inch milk pan and a 26-inch mathar kadai, distributed to customers in multiple states. The FDA enforcement report notes elevated lead levels in the products. Consumers should stop using the cookware and contact Goyal Group for a refund or replacement.

Goyal Group
Contains elevated
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet 15lb Bulk Madison Mix Recalled Over Undeclared Allergens

Taproom Gourmet recalled 3,547 cases of 15lb bulk Madison Mix after undeclared allergens were found. The recall cites no ingredient label as the defect. Consumers should not consume the product and should seek refund or replacement from Egress Capital Partners Inc.

Taproom Gourmet
No ingredient
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Food & Beverages
HIGH
FDA FOOD

Taproom Gourmet Bulk Fifth Avenue Mix Recalled for No Ingredient Label and Allergens

Taproom Gourmet recalled 3,547 cases of 18lb and 20lb bulk Fifth Avenue Mix sold in six states after undeclared peanuts, almonds, cashew, and soy were found. The recall classifies the hazard as HIGH. Consumers should discard the product or return for refund or replacement via Egress Capital Partners Inc.

Taproom Gourmet
No ingredient
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Food & Beverages
HIGH
FDA FOOD

Lawrence Wholesale Shrimp Cocktail Bowls Recalled for Cs-137 Contamination Risk (2025)

Lawrence Wholesale recalled 8,400 cases of Shrimp Cocktail Bowl products sold to Kroger stores in 15 states on Sept. 16, 2025 due to potential Cesium-137 contamination. The recall involves 7oz and 17oz clear plastic bowls with UPCs 011110622952 and 011110624840. Consumers should not consume the product and should contact Lawrence Wholesale LLC for refund or replacement by email.

Lawrence Wholesale
Product manufactured
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