All Product Recalls

Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Food & Beverages
HIGH
FDA FOOD

Arctic Shores Frozen Cooked Salad Shrimp Recalled in 93,122 Cases Over Cs-137 Contamination (2025)

Arctic Shores recalled 93,122 cases of Frozen cooked salad shrimp in 6 oz bags. The recall affects products distributed to 26 states. The product may be contaminated with Cesium-137 due to insanitary manufacturing conditions. Consumers should not eat this product and should contact Southwind Foods LLC dba Great American Seafood Imports for refund or replacement information.

Arctic Shores
Product manufactured
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Food & Beverages
HIGH
FDA FOOD

Arctic Shores Frozen Shrimp Recall Expanded for Cs-137 Contamination (2025)

Southwind Foods LLC dba Great American Seafood Imports Co. expanded recall covers Arctic Shores, Best Yet, Great American and Master Catch frozen shrimp sold nationwide by multiple retailers after Cesium-137 contamination was detected. The contaminated product was manufactured under insanitary conditions. Consumers should not eat the product and should contact the company for refunds or replaced.

Arctic Shores
Product manufactured
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Health & Personal Care
HIGH
FDA DEVICE

BD Phoenix M50 Recall: 4,283 Systems Worldwide Over Access Risk (2025)

BD recalled 4,283 Phoenix M50 Automated Microbiology Systems worldwide after unauthorized access to product service credentials. The unauthorized actor could access affected products and data. Labs should stop using these devices and follow the recall instructions from BD; contact BD for remediation guidance.

BD
Product service
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Food & Beverages
HIGH
FDA FOOD

Tengen USA Trading Recalls Cucumber Product Over Cyclamate Hazard

Tengen USA Trading Corp recalled 26 cases of YO!MAN Cucumber (Fresh Hunan Flavor) on September 23, 2025, due to undeclared cyclamates. The product poses a high risk of poisoning for consumers allergic to this chemical. Consumers should not consume the product and seek refunds.

TENGEN USA TRADING
Product contains
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Food & Beverages
HIGH
FDA FOOD

Tengen USA Trading Recalls YO!MAN Lettuce Over Undeclared Cyclamates

Tengen USA Trading Corp recalled YO!MAN Lettuce (Spicy Flavor) on September 23, 2025. The product contains undeclared cyclamates, posing health risks. This recall affects 26 cases distributed across several states, including New York and Texas.

TENGEN USA TRADING
Product contains
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Food & Beverages
HIGH
FDA FOOD

Sea Port Jumbo Shrimp Recalled for Cs-137 Contamination in 2025

Sea Port brand Raw Frozen Easy Peel Headless Shell-On White Shrimp, Jumbo 16-20, distributed by Sea Port Products Corp in Kirkland, WA, is recalled. A Cs-137 contamination risk is identified. About 1,800 cases are affected across two master-case configurations. Consumers should not consume the product and should contact Sea Port for refunds or replacements.

Sea Port Products
Shrimp may
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls 160 DxC 500i Modules and DxI 9000 Analyzers in 2025 Recall

Beckman Coulter recalls 160 DxC 500i Clinical Analyzer Modules and the DxI 9000 Access Immunoassay Analyzer worldwide after a software anomaly could misapply manual dilution factors. The defect affects samples already in progress using the same Sample ID. Stop using the devices immediately and follow the recall instructions. Beckman Coulter will provide instructions via the recall process.

Beckman Coulter
Beckman Coulter
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Health & Personal Care
HIGH
FDA DRUG

Ascend Laboratories Recall Atorvastatin Calcium 40 mg Tablets for Failed Dissolution Specifications

Ascend Laboratories recalled Atorvastatin Calcium Tablets USP 40 mg, 90-count (NDC 67877-513-90), 500-count (NDC 67877-513-05), and 1,000-count (NDC 67877-513-10) nationwide in the United States. The batches failed dissolution specifications. Patients should stop using the medication and contact Ascend Laboratories, LLC or their healthcare provider for guidance.

Atorvastatin Calcium
Failed Dissolution
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalled 14,220 Dozen Free Range Eggs Over Salmonella Risk (2025)

Black Sheep Egg Company recalled 14,220 dozen Free Range Grade AA Medium Brown Eggs after FDA notice of potential Salmonella contamination. The recall covers loose-pack boxes sold at retail and wholesale locations in Arkansas and Missouri, with wholesale distribution to Mississippi, Texas, California and Indiana. Consumers should not consume the eggs and should contact the company for refunds or替换

Black Sheep Egg Company
Potential Salmonella
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Health & Personal Care
HIGH
FDA DRUG

Ascend Laboratories Recalls Alkem Atorvastatin Calcium 20 mg Tablets for Dissolution Failures (3 NDC

Ascend Laboratories recalls Alkem Atorvastatin Calcium Tablets USP 20 mg for dissolution failures in 2025. Distributed by Ascend Laboratories, Parsippany, NJ, nationwide. The issue: dissolution specifications not met. Stop use immediately and follow recall instructions. Check your NDC numbers to identify affected lots.

Ascend Laboratories
Failed Dissolution
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Health & Personal Care
HIGH
FDA DRUG

ATORVASTATIN CALCIUM Tablets 10 mg Recall: 141,984 Bottles Nationwide (2025)

Ascend Laboratories, Parsippany, NJ is recalling 141,984 bottles of ATORVASTATIN CALCIUM Tablets USP, 10 mg, nationwide, manufactured by Alkem Laboratories, Ltd. in India. The issue is failed dissolution specifications, which could lead to improper dosing. Healthcare providers and patients should stop using the product and contact Ascend Laboratories for guidance.

ATORVASTATIN CALCIUM
Failed Dissolution
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls 571 DxI 9000 Immunoassay Analyzers and DxC 500i (2025)

Beckman Coulter recalled 571 DxI 9000 Access Immunoassay Analyzers and DxC 500i Clinical Analyzers distributed worldwide. A software anomaly may prevent correct application of manual dilution factors for tests already in progress on the same Sample ID. Labs should stop using the devices immediately and follow recall instructions.

Beckman Coulter
Beckman Coulter
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Free Range Grade AA Eggs Recalled for Salmonella Risk (20,625 Dozen) 2025

Black Sheep Egg Company recalled 20,625 dozen eggs sold at retail and wholesale locations in Arkansas and Missouri after a potential Salmonella contamination. The eggs are Free Range Grade AA Large Brown, loose-packed in boxes. Consumers should not consume these eggs and should contact Black Sheep Egg Company for refunds or replacements.

Black Sheep Egg Company
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Shell Eggs Recall 2025 for Salmonella Contamination

Black Sheep Egg Company recalled Free Range Grade AA Large White Shell Eggs after Salmonella contamination concerns were identified. The recall covers 7,200 dozen eggs distributed to retail and wholesale locations in Arkansas and Missouri, with brokered sales in Mississippi, Texas, California and Indiana. Consumers should not consume these eggs and should contact the company for refund or refund/替

Black Sheep Egg Company
Potential Salmonella
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recall: 288,900 Dozen Free Range Grade AA Eggs Over Salmonella Risk

Black Sheep Egg Company is recalling 288,900 dozen Free Range Grade AA Large Brown Eggs sold at retail and wholesale locations in Arkansas and Missouri, with broker distribution in Mississippi, Texas, California and Indiana. The recall cites potential Salmonella contamination as the hazard. Consumers should not consume these eggs and should contact Black Sheep Egg Company for refund or replacement

Black Sheep Egg Company
Potential Salmonella
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