2,056 recalls tagged with “cpsc regulated”.
Dr. Reddy's Laboratories recalled 4,800 bottles of Varenicline tablets on November 11, 2025, due to sub potent drug levels. The affected lot failed stability tests, posing potential health risks to users. Consumers should stop using the product immediately and consult healthcare providers.
Olympus Corporation of the Americas recalled 2,626 units of its Resection Sheath on November 11, 2025. The ceramic tip of the sheath may break during use, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.
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.
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 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.
Draeger recalled 2,050 units of the ErgoStar CM 60 airway connector on November 10, 2025. The recall follows multiple reports of cracks in the device, posing a risk to mechanically ventilated patients. Healthcare providers and patients should stop using the connector immediately.
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.
Kosher First recalled 283 units of Shloimy's Heimishe Matjes Herring on November 10, 2025, due to undeclared FD&C Red #40. The recall affects products distributed in New York and poses a high risk of allergic reactions. Consumers should not consume the product and seek refunds or replacements.
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.
Toyota Motor Engineering & Manufacturing recalls multiple 2023-2025 vehicles because the instrument panel may fail to display speed, braking and tire pressure alerts. Dealers will update software for non-PHEV models and inspect/possibly replace panels for PHEV models at no charge. Owner letters expected Oct 27, 2025. Contact Toyota at 1-800-331-4331; Lexus follow numbers 25LB05/25LA05.
Pacific Seafood recalled 15,498 pounds of Raw Blackened Shrimp Peeled & Deveined Tail-Off sold refrigerated after undeclared sulfite was detected. The product is a shrimp tray produced in Ecuador and distributed in Alabama, Florida and Massachusetts. Consumers should not eat the product and should contact Pacific Seafood Group for a refund or replacement.
Ford Motor Company recalled 2023 Lincoln Corsair, 2023-2024 Escape, 2024 Mustang, and 2025 Explorer vehicles due to fuel injector assembly lacking O-ring support discs. The defect may cause a fuel leak with ignition risk. Dealers will install new fuel injector O-rings and O-ring support discs at no charge. Owner letters mailed Oct 7, 2024. Ford contact: 1-866-436-7332. Recall number 24S54.
Costco Wholesale recalled 612 units of Kirkland Signature Chicken Sandwich with Caesar Salad distributed in New York and Puerto Rico. The 3-ounce Caesar Dressing packet in the sandwich may contain plastic material. Consumers who bought the product should not consume it and should contact Costco for a refund or replacement.
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.
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.
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.
Gulf States Toyota, Inc. recalls 2025 Camry Hybrid vehicles equipped with GST accessories after discovering load carrying capacity labels may display inaccurate added weight values. The mislabeling could cause the vehicle to be overloaded, increasing the risk of a crash. Owners should contact GST for a free label replacement; letters were mailed September 16, 2024.
Bard Peripheral Vascular recalled 1,240 Safe-T-Centesis Catheter Drainage Trays due to safety indicator defects. The recall affects products distributed nationwide since November 6, 2025. The defect may cause serious injuries during use in medical procedures.
C.R. Bard recalled 4,350 units of the InLay Optima Ureteral Stent Kit on November 6, 2025. The recall was initiated due to a labeling discrepancy where the actual size of the stent may not match its label. This affects distribution across the U.S. and several countries worldwide.
Napei recalled its collapsible infant bath tubs sold on Amazon by Sefon Store after discovering the built-in thermometer uses button cell batteries that are accessible to children. The batteries pose a risk of ingestion, which can cause serious injuries or death. Stop using the tub immediately and contact Sefon Store for a free replacement battery compartment.