These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,775 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Exela Pharma Sciences recalled 4.2% Sodium Bicarbonate Injection on July 30, 2025, due to arsenic contamination. The recall affects single-dose vials distributed nationwide. Consumers and healthcare providers must stop using the product immediately.
Contract Medical International GmbH recalled 2,500 Fortress Introducer Sheath Systems on July 30, 2025. Units may have incorrect pouch labeling, leading to potential use of the wrong device version. Patients and healthcare providers should stop using the product immediately.
S.I.N. Implant System Ltda recalled 4,367 dental implants on July 30, 2025, due to improper storage conditions. The recalled products may have compromised packaging, affecting their quality and performance. Patients and healthcare providers should stop using these devices immediately.
Pfizer Inc. recalled 29,004 bottles of Levoxyl on July 29, 2025, due to subpotency. The recall affects levothyroxine sodium tablets, 50 mcg, Rx only, distributed in the U.S. Consumers should stop using the product immediately.
Ortho-Clinical Diagnostics recalled 2,908 units of VITROS Chemistry Products LAC Slides on July 29, 2025. The recall affects lots from coating 0130 and above due to increased calibration failures that delay test results. The issue may impact patient management and was identified through an uptick in customer complaints.
Ortho-Clinical Diagnostics recalled 2,320 units of VITROS Chemistry Products LAC Slides on July 29, 2025. Calibration failures in lots from coating 0130 and above delay test results and may impact patient management. Healthcare providers and patients must stop using these slides immediately.
American Health Packaging recalled 26,992 blister packs of Sucralfate Tablets on July 29, 2025. The recall follows CGMP deviations that affect product quality. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Dynamic Sports Nutrition recalled 1,566 bottles of WINN-50 dietary supplement on July 28, 2025. The product contains sub-potent levels of Vitamin B12, failing to meet label claims. Consumers should stop using the product immediately and seek refunds.
ORTOMA AB recalled 261 Inserter Adapters on July 28, 2025, due to a potential weld failure. The defect poses a risk of improper positioning during hip implant procedures. The recall affects devices distributed worldwide, including the U.S. and countries like Japan and Sweden.
Medline Industries, LP recalled 2,520 medical convenience kits on July 25, 2025. The recall affects multiple intubation trays containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. The light in these devices fails to illuminate, posing a serious risk in emergency situations.
Merit Medical Systems recalled 447 units of the 10Fore Hemostasis Valve on July 25, 2025. A manufacturing issue may cause a deformed silicone quad ring, posing a risk of foreign body in the fluid pathway. This recall affects the U.S. and Canada.
Medline Industries, LP recalled 596 medical convenience kits on July 25, 2025. The recall affects kits with Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to light failure. Patients and healthcare providers must stop using these devices immediately.
Towa Pharmaceutical Europe recalled 1,856 bottles of Duloxetine delayed-release capsules on July 25, 2025. The recall follows the discovery of N-nitroso-duloxetine impurity exceeding FDA limits. Consumers should stop using the product immediately and seek guidance.
Gelson's recalled 7,861 units of its Low Sodium No Cholesterol Classic Hummus on July 25, 2025. The product labels fail to include essential storage instructions to keep refrigerated. Consumers should not consume the product and seek a refund.
Gelson's recalled 7,861 units of Red Bell Pepper Hummus on July 25, 2025. Labels failed to include critical storage instructions to keep refrigerated. Consumers should not consume the product and seek refunds.
Zap Surgical Systems recalled 17 ZAP-X Radiosurgery Systems on July 25, 2025. A software defect may cause the collimator to collide with patients during operation. Healthcare providers should stop using the device immediately.
Home Health US recalled 4,661 sterile lancets on July 25, 2025. The recall stems from incorrect or missing Unique Device Identifier (UDI) codes. Affected products were distributed nationwide through Amazon.
iMirror Inc. recalled its Electric Bug Zapper Racket, Fly Swatter, and Mosquito Swatter on July 24, 2025. The rechargeable battery can catch fire during extended use. Consumers should stop using the products and contact iMirror for a full refund.
Innovative Designs recalled Minecraft Light-Up Slap Ruler Bracelets on July 24 due to a serious ingestion hazard. The product's battery compartment can be easily opened by children, exposing button cell batteries. This poses a risk of serious injury or death.
LIVACTI recalled retractable safety gates on July 24, 2025, due to serious entrapment hazards. The gates can pose a risk of injury or death to children. Consumers should stop using them immediately and seek refunds.