612 recalls tagged with “poisoning risk”.
MAYEJ COMERCIALIZADORA S. de R.L. de C.V. recalled 1,288 boxes of Italian Parsley on September 26, 2025. The recall follows concerns over contamination with Cyclospora cayetanensis, a harmful pathogen. Consumers should avoid consumption and seek refunds immediately.
Mad Rabbit recalls RELIEVE lidocaine numbing cream due to non‑compliant packaging that could allow poisoning of young children. The recall covers a product sold under the Mad Rabbit brand and issued on 2025-09-25. The packaging does not meet the Poison Prevention Packaging Act requirement for child resistance. Consumers should stop using the product immediately and contact Mad Rabbit for a free, a
Aloe Up recalled 11,386 tubes of Aloe Up Sport Performance Sunscreen Lotion SPF 30 sold nationwide in the United States. The recall cites cGMP deviations after the product failed total aerobic microbial count testing. Consumers should stop using the product and follow guidance from SV Labs Prescott Corporation or a healthcare provider.
Audi and Volkswagen Group of America recall 2025 GTI, Golf R, Audi A5, A6 Sportback E-Tron, S5, S6 Sportback E-Tron, 2026 Q4 Sportback E-Tron and Q4 E-Tron vehicles. The torsion bar in the front seat belt retractors may be damaged during production. Dealers will replace one or both front seat belts at no charge. VIN lookups begin Sept 26, 2025 and owner letters go out Nov 21, 2025.
Ent ecavir 0.5 mg tablets, distributed nationwide in the United States by Zydus Pharmaceuticals USA Inc., are recalled, affecting 912 bottles. The recall is due to an out-of-specification organic impurity detected in a batch, Class II. Healthcare providers and patients should stop using the product immediately and contact Zydus Pharmaceuticals USA for guidance.
NOW Foods recalled 1,689 10 oz pouches of NOW Real Food Organic Unsalted Whole Raw Cashews nationwide after undeclared pine nuts were detected. The hazard poses an allergen risk. Consumers who bought this product should stop using it and contact NOW Foods for a refund or replacement.
Zydus Lifesciences and Zydus Pharmaceuticals USA recall 600 bottles of Entacavir 1 mg tablets distributed nationwide in the United States. An out-of-specification organic impurity triggered the recall. Stop use immediately and contact a healthcare provider or Zydus for guidance.
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 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.
Great American Seafood Imports recalled 93,122 cases of its frozen raw shrimp skewers after potential Cs-137 contamination. The recall expansion cites insanitary manufacturing conditions. Consumers should not consume the product and should contact the company for refund or replacement.
El Rojo Wholesale recalled 2,904 units of El Rojo Pasta De Harina, Wheat Pellets, distributed in Minnesota. The recall cites missing ingredient information and no nutritional panel. Consumers should not eat the product and should contact the company for refund or replacement.
Southwind Foods LLC, doing business as Great American Seafood Imports, recalled 93,122 cases of Tovala-brand frozen raw phosphate-free shrimp after identifying potential Cesium-137 contamination. The recall expands a prior action and notes insanitary production conditions. Consumers who bought the 5 oz IQF bag with UPC 829944085788 should not eat it and should contact the supplier for refund or re
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 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.
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.
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 recalls 58,500 dozen free range Grade AA medium brown eggs after FDA enforcement notice citing potential Salmonella contamination. The recall covers eggs sold in Arkansas and Missouri, with wholesale and broker locations in Mississippi, Texas, California and Indiana. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refund or replacement.
Black Sheep Egg Company recalled 23,400 dozen Free Range Grade AA Large White Eggs sold at retail and wholesale locations in Arkansas and Missouri due to potential Salmonella contamination. Consumers should not eat these eggs. Contact Black Sheep Egg Company, LLC for refund or replacement information.
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
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.