2,715 recalls tagged with “immediate action”.
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.
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 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.
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 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.
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.
Hospira, Inc. recalled 49,620 vials of Epinephrine Injection on August 4, 2025. The recall follows concerns about the lack of assurance of sterility. Consumers should 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.
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.
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.
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.
AVID Medical recalled 228 units of the Halyard CPT BASIC IR Pack on August 4, 2025. The recall follows reports of open header bag seals that may compromise sterility. Healthcare providers and patients should stop using the device immediately.
B. Braun Medical Inc. recalled 74,088 containers of Lactated Ringer's Injection on August 4, 2025. The recall stems from a lack of assurance of sterility and potential fluid leakage. Consumers and healthcare providers should discontinue use immediately and seek guidance.
Hans Kissle Company recalled 66 units of Red Bliss Potato Salad on August 4, 2025, due to undeclared wheat. The product is mislabeled as potato salad but contains pasta salad. Consumers should not eat the product and should seek a refund or replacement.
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.
Beckman Coulter recalled 116 DxC 500i Clinical Analyzer modules on August 4, 2025, due to potential processing delays. The defect may impact the accuracy of test results when ordering certain tests simultaneously. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
DFA Dairy Brands recalled 54 cases of Friendly's Ice Cream on August 1, 2025. The product contains undeclared wheat and soy, posing a serious allergen risk. Consumers in Maryland, Virginia, and Pennsylvania should not consume the affected ice cream.
Dorel Home Furnishings recalled Cosco 2-step kitchen steppers on July 31, 2025. The safety bar can detach, posing fall risks. Consumers should stop using the product and seek repairs immediately.
IKEA recalled garlic presses on July 31, 2025, after reports of small metal pieces detaching. The recall affects the IKEA 365+ VÄRDEFULL models with the IKEA logo. Consumers should stop using these products immediately and return them for a refund.