1,862 recalls tagged with “stop use immediately”.
AMTRADING recalled Cooling Gel Insert Pads on September 25, 2025, after reports of burn hazards. The pads can become hot if left in the sun or a hot car, posing a risk to children. Consumers must stop using the product and contact AMTRADING for a full refund.
Persilux recalled zebra blinds on September 25, 2025, due to strangulation and entanglement hazards. The recalled blinds pose a serious risk of injury or death to children. Consumers should stop using the blinds immediately and contact Persilux for a repair kit.
Sunbeam Products recalled more than one million Oster French Door Countertop Ovens on September 25, 2025. The recall affects models TSSTTVFDXL, TSSTTVFDDG, TSSTTVFDMAF, and TSSTTVFDDAF due to a burn hazard from doors that can unexpectedly close. Consumers should stop using the ovens and contact Sunbeam for a free repair kit.
Georgia Nut Co recalled 76,121 cases of tru fru Strawberries + Creme on September 25, 2025. The recall follows reports of potential metal contamination in the product. Consumers should stop using the product immediately and seek a refund or replacement.
LeMaitre Vascular recalled one unit of its Collagen Vascular Graft on September 25, 2025. The device was packed in the wrong size labeled outer packaging, posing a high hazard to patients. Health providers and patients should stop using this device immediately and follow the recall instructions.
DJO recalled 1,594 cold compression wraps on September 25, 2025. The wraps may leak or break when heated in the microwave, posing a burn risk. The recall affects models REF: DP163CT03-BLK-L, XL, and DP163CT02.
Zydus Pharmaceuticals recalled 912 bottles of Entecavir Tablets on September 24, 2025, due to failed impurity specifications. The recall affects 30-count bottles of 0.5 mg tablets Distributed nationwide in the USA.
Becton Dickinson & Co. recalled 177 units of the BD BACTEC Blood Culture System on September 23, 2025. Unauthorized access to product service credentials poses a high risk to patient data and device integrity. Healthcare providers must stop using the devices immediately and follow recall instructions.
OptiWize Health recalled 78 units of its Collagen Plus supplement on September 23, 2025. Testing revealed discrepancies in labeled ingredient quantities, particularly lower manganese levels. Consumers should not consume the product and contact the company for refunds.
Tovala recalled 93,122 cases of frozen shrimp on September 23, 2025. The product may have been contaminated with Cesium-137. Consumers should stop using the product immediately and seek a refund.
Scott & Jon's Honey Sesame Salmon Rice Bowl is recalled due to undeclared wheat. The recall affects 966 cases distributed across multiple states. Consumers should stop using the product and contact the manufacturer for refunds.
Becton Dickinson recalled 62 units of its BD MAX System on September 23, 2025. Unauthorized access to product service credentials poses a high risk to data confidentiality and system integrity. The recall affects worldwide distribution, including the U.S., and requires immediate action from users.
Biomet recalled 98 units of its ZipTight Acute AC Joint Implant on September 23, 2025. The recall follows reports of a potential missing slotted button assembly in one lot. Patients and healthcare providers must stop using the device immediately.
Becton Dickinson & Co. recalled 2,050 units of its EpiCenter Microbiology Data Management System on September 23, 2025. Unauthorized access to product service credentials may compromise patient data. The recall affects models distributed worldwide, including the U.S. and Puerto Rico.
Becton Dickinson & Co. recalled 1,086 units of its BACTEC Blood Culture System on September 23, 2025. Unauthorized access to product service credentials poses a risk to data security. Affected systems include the BACTEC 9120 with catalog numbers 445570 and 445702.
Becton Dickinson & Co. recalled 38 units of BD Veritor Connect Software on September 23, 2025. Unauthorized access to product service credentials may compromise data confidentiality and integrity. Users must stop using the software immediately and follow recall instructions.
Arctic Shores recalled 93,122 cases of frozen cooked salad shrimp on September 23, 2025. The product may contain Cesium-137, a radioactive isotope. Consumers should stop using the product immediately and seek refunds.
RC Outsourcing LLC recalled 2,669 syringes of Bevacizumab on September 22, 2025. The recall stems from a lack of assurance of sterility, raising significant health risks. Healthcare providers and consumers should stop using the product immediately.
Sea Port Products Corporation recalled 1,800 cases of Raw Frozen Easy Peel Headless Shell-On White Shrimp. The recall follows concerns about contamination with Cesium-137. Consumers should stop using the product immediately.
Ascend Laboratories recalled atorvastatin calcium tablets on September 19, 2025, due to failed dissolution specifications. The recall affects 90-count, 500-count, and 1000-count bottles. Consumers should stop using these medications immediately.