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.
2,247 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Hi-Tech Pharmaceuticals recalled 85,950 units of Slimaglutide on August 6, 2025. The recall is due to unapproved drug claims and misbranding. Consumers should stop using the product immediately and seek a refund or replacement.
The Candy Barn recalled 665 packages of Grandma's Old-Fashioned Peanut Brittle on August 6, 2025. The packaging failed to list peanuts and milk as allergens. Consumers should avoid the product and seek a refund.
The Candy Barn recalled 665 packages of Chocolate Walnut Fudge on August 6, 2025. The product does not list walnut and egg allergens in the 'contains' statement. Consumers should not consume the fudge and seek refunds or replacements.
The Candy Barn recalled 665 packages of Peanut Butter Fudge on August 6, 2025. The product contains undeclared egg allergens not listed in the labeling. Consumers should not consume this fudge and seek a refund or replacement.
Olympus Corporation of the Americas recalled 103,731 units of the ViziShot 2FLEX aspiration needle on August 6, 2025. The recall stems from a risk of undetected, deformed a-traumatic tips that could affect patient safety. The product is distributed worldwide, including the US, Australia, and Germany.
Glenmark Pharmaceuticals recalled 17,496 bottles of Carvedilol Tablets on August 6, 2025. Tests revealed N-Nitroso Carvedilol Impurity-1 levels exceeded FDA limits. Consumers should stop using the medication immediately.
Glenmark Pharmaceuticals recalled 14,976 bottles of Carvedilol Tablets on August 6, 2025. The recall follows findings of N-Nitroso Carvedilol Impurity-1 above FDA limits. Consumers should stop using the product immediately and contact their healthcare provider.
Sandoz Inc. recalled 10 bags of Enoxaparin Sodium Injection on August 5, 2025. Bags labeled for Enoxaparin Sodium 80 mg/0.8 mL contained the incorrect dosage of 30 mg/0.3 mL. Consumers and healthcare providers must stop using the product immediately.
M.O.M Enterprises recalled 85,248 units of its Organic BABY bedtime drops due to potential yeast contamination. The recall affects two lots sold nationwide since August 2025. Consumers should stop using the product immediately and seek a refund.
Philips Medical Systems recalled 810 units of its Radiation Therapy Planning System on August 5, 2025. A software issue may cause image errors during treatment planning. Affected models include Pinnacle TumorLOC and Multimodality Simulation Workspace.
Boston Scientific recalled 458 NephroMax Kits on August 5, 2025, due to contamination risk. The Encore 26 Inflation Device may allow foreign particles to enter balloon dilatation catheters. Patients must stop using the device immediately and follow recall instructions.
Boston Scientific recalled 1,369 UroMax Ultra Kits on August 5, 2025. Foreign particles may migrate from the Encore 26 Inflation Device into balloon dilation catheters. Patients and healthcare providers must stop using the device immediately.
Boston Scientific recalled 39,739 Encore 26 Inflation Devices on August 5, 2025. Foreign particles may migrate into balloon dilation catheters during use. Patients and healthcare providers must stop using the device immediately.
Haleon US Holdings recalled 46,692 tubes of Sensodyne PRONAMEL toothpaste on August 5, 2025, due to a labeling mix-up. The outer carton states Fresh Mint while the tube claims Cool Mint/Whitening. The actual product inside is Fresh Mint, leading to potential consumer confusion.
Tandem Diabetes Care recalled 122,958 insulin pumps on August 5, 2025. A software defect may cause unexpected insulin boluses, leading to hypoglycemia. Patients should stop using the devices immediately and follow the manufacturer's instructions.
B. Braun Medical Inc. recalled 23,100 containers of 0.9% Sodium Chloride Injection on August 4, 2025. The recall stems from a lack of assurance of sterility and potential fluid leakage. This product is distributed nationwide in the United States.
Hospira, Inc. recalled 15,750 vials of Sodium Bicarbonate Injection on August 4, 2025. The recall stems from a lack of assurance of sterility. Consumers and healthcare providers must stop using the product immediately.
AVID Medical recalled 57 units of the Halyard ENT Pack on August 4, 2025. The recall stems from potential open header bag seals that may compromise sterility. Patients and healthcare providers must stop using this device immediately.
Wasatch Photonics recalled 192 Raman spectrometers on August 4, 2025. Two potential laser safety failure modes could pose serious risks. No incidents have been reported, but excessive force or vibration may trigger failures.
Neuhaus nv recalled 100 pieces of ORIGINAL BELGIAN CHOCOLATE on August 4, 2025, due to undeclared wheat. The recall affects products distributed in Virginia, Maryland, Pennsylvania, New York, and Washington D.C.