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.
2,251 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Draeger recalled 191,470 units of the ErgoStar CM 45 airway connector on November 10, 2025. Users reported cracks in the hose of specific catheter mounts, posing a high risk to patients. The recall affects healthcare facilities worldwide, including multiple U.S. states.
Draeger recalled 14,420 units of its ErgoStar CM 40 airway connector on November 10, 2025, due to cracks forming in the hose. The recall affects multiple states in the U.S. and several countries worldwide.
Waldemar Link GmbH & Co. KG recalled 18 units of the Endo Model Knee Fusion Nail SK on November 10, 2025. The device features a preassembled locking screw incorrectly inserted, posing a high risk of failure. Affected units were distributed in Alabama, Georgia, and Texas.
Draeger recalled 118,850 airway connectors on November 10, 2025, due to cracking hazards. This recall affects multiple countries, including the United States and Australia. The device poses a serious risk to mechanically ventilated patients.
Beckman Coulter recalled 76,098 units of COULTER DxH Diluent on November 10, 2025. The recall affects specific lots contributing to elevated platelet background counts in analyzers. Healthcare providers and patients must stop using this product immediately.
Chrysler is recalling certain 2022-2025 Jeep Wagoneer and Grand Wagoneer vehicles. Improperly installed trim on the driver and passenger doors may detach, creating a road hazard. The recall affects an unknown number of vehicles manufactured through 2025.
Toyota recalled the 2025 Camry due to a software issue that affects the instrument panel. The malfunction can obscure critical driving information, increasing crash risk. Notification letters will be sent to owners by October 27, 2025.
Ford Motor Company recalled the 2025 Explorer on November 8, 2025. The recall affects vehicles with fuel injectors potentially lacking O-ring support discs. A fuel leak could increase the risk of fire.
Pacific Seafood recalled 15,498 pounds of Raw Blackened Shrimp on November 8, 2025. The shrimp may contain undeclared sulfites, posing a health risk to sensitive individuals. The affected products were distributed in Alabama, Florida, and Massachusetts.
ByHeart announced a recall of over 6.9 million units of its infant formula on November 8, 2025, due to contamination with Clostridium botulinum. The recall affects both cans and single-serve packets sold nationwide. Parents are urged to stop using the affected products immediately to prevent serious health risks.
Gulf States Toyota is recalling 2025 Camry Hybrid vehicles due to incorrect load capacity labels. The recall affects an unspecified number of vehicles sold since 2023. Faulty labels may lead to overloading and increase crash risk.
Actavis Laboratories recalled 15,944 cartons of Testosterone Gel on November 7, 2025. The recall follows a defect in the side-seal of the containers, which may allow product leakage. Consumers must stop using the product immediately and contact their healthcare providers for guidance.
Costco recalled 612 units of its Kirkland Signature Chicken Sandwich with Caesar Salad on November 7, 2025. The product may contain plastic material in the Caesar dressing packet. Consumers should not consume this product and seek refunds immediately.
Costco recalled 142,532 units of Kirkland Signature Caesar Salad on November 7, 2025. The salad's dressing packet may contain plastic material, posing a choking hazard. Affected products have sell-by dates between October 17, 2025, and November 9, 2025.
Beckman Coulter recalled 38,225 Access 2 Reaction Vessels on November 7, 2025, due to manufacturing deformities. These defects can cause instrument errors that delay patient results. Healthcare providers and patients should stop using the affected vessels immediately.
Anthony's Barbecue & Dip-It Sauce is recalled due to an undeclared fish allergen. The recall affects 192 glass bottles with UPC 6 89076 62272 1. Consumers should not consume the sauce and contact the company for a refund.
Intuitive Surgical recalled 219 da Vinci surgical systems on November 7, 2025, due to a software error. This error allowed malfunctioning instrument arms to remain in clinical use, posing a high risk of failure. Healthcare providers and patients must stop using these systems immediately.
Fresenius Kabi USA, LLC recalled 2,199,850 vials of Famotidine Injection on November 6, 2025. The recall follows reports of microbial contamination and endotoxin testing failures. Healthcare providers and consumers should stop using this product immediately.
Napei recalled infant bath tubs on November 6, 2025, due to a serious ingestion hazard. The tubs contain button cell batteries that can be accessed by children, posing risks of internal burns and death. Consumers should stop using the product immediately and contact the retailer for a replacement battery compartment.
Neaude recalled adult portable bed rails on November 6, 2025, due to serious injury and death risks. The model BR0221SL001 poses an entrapment hazard that can lead to asphyxiation. Consumers should stop using the product immediately and seek a refund.