1,003 recalls tagged with “chemical 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 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.
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.
Over 93,000 cases of Arctic Shores frozen raw shrimp have been recalled due to potential contamination with Cesium-137. The shrimp were manufactured under insanitary conditions that raise serious health concerns. Consumers should not consume this product and should seek a refund from Great American Seafood Imports.
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.
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.
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.
Arizer recalled the Solo II portable vaporizer on 2025-09-18 after reports of overheating lithium-ion batteries. The recall targets units imported by 7111495 Canada. Consumers should stop using the device and pursue a free replacement.
YooxArmor recalled its multi-purpose kids’ helmets sold on Amazon after safety violations. The helmets fail to meet the mandatory bicycle helmet standard for impact attenuation, stability, labeling and certification. Consumers should stop using the helmets and request a full refund from YooxArmor.
LXDHSTRA recalled baby loungers and crib bumpers on September 18, 2025. The recall covers LXDHSTRA-branded loungers sold online at Amazon. The defect involves suffocation and fall hazards linked to design and ban violations. Stop using immediately and seek a full refund from LXDHSTRA.
Five Below recalls two tabletop fire pits after reports of alcohol fuel flames jetting and spreading. The recall affects devices sold nationwide. Stop using the recalled pits immediately and contact Five Below for a refund. Full refunds available or $5 option; mail-back refunds possible with photo submission.
B Braun Medical has an active recall of the PERIFIX FX Continuous Epidural Anesthesia Tray nationwide. The recall cites a potential mispositioned catheter connector lid. Healthcare providers and patients should stop using the device and follow manufacturer instructions.
B Braun Medical recalled an epidural anesthesia tray nationwide after finding a lid misalignment in the catheter connector could occur. The recall involves the PERIFIX FX Continuous Epidural Anesthesia Tray and PERIFIX FX Springwound Catheter with a 17 Ga Tuohy needle and 19 Ga closed-tip catheter. The recall date is 2025-09-18 with report of ongoing action as of 2025-10-15. Healthcare providers,,
B Braun Medical recalled 2,450 SESK pain management trays distributed nationwide. The recall cites a potential mispositioned catheter connector lid, classified as Class II with high hazard. Patients and healthcare providers were advised to stop using the device and follow recall instructions.
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.
Kirkland Signature Ahi Tuna Wasabi Poke sold at Costco is recalled after a Listeria monocytogenes positive test in green onions used in the product. Western United Fish Company initiated the recall. Consumers should not eat the product and should seek refunds or replacements.
B Braun Medical recalled 10,130 ESPOCAN spinal/epidural trays nationwide after discovering potential for the catheter connector lid to be in an incorrect position. The recall covers multiple product codes and UDI numbers. Healthcare providers must stop using affected units and follow manufacturer instructions for remediation.
Taproom Gourmet bulk Park Mix, distributed to NY, NJ, CT, CA, IL and FL, is recalled for undeclared allergens and no ingredient label. Consumers should not consume the product. Egress Capital Partners Inc. is handling refunds or replacements via email.
B BRAUN MEDICAL INC recalls 2,760 units nationwide due to a lid misalignment risk in the catheter connector. The recall covers the PERIFIX FX Continuous Epidural Anesthesia Tray and related components. Healthcare providers should halt use and follow manufacturer instructions for recall remedies.
B BRAUN MEDICAL INC recalls 60 units of SESK Combined Spinal and Epidural Tray nationwide. The recall targets products distributed to all 50 states. The defective lid on the catheter connector may be in the incorrect position, posing a high-risk device issue. Stop using immediately and follow company instructions for recall remedies.