1,814 product recalls found in this category. Browse through all safety alerts and stay informed.
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This category has a significant number of recalls. Please check regularly for updates.
Applied Medical Technology recalled 200 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. The distal tips may detach at lower than expected forces. Stop using the device immediately and follow the manufacturer’s recall instructions.
Agilent Technologies recalled 65 FLEX Monoclonal Mouse Anti-Human CD20cy antibodies distributed nationwide in the United States. The recall cites weak staining that may yield false negative CD20 results. Labs and healthcare providers should stop using the product immediately and follow the manufacturer’s recall instructions.
Agilent Technologies Denmark ApS recalled 4,145 FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use antibodies distributed nationwide in the United States. The defect is a potential for weak staining that can yield a false negative CD20 result. Labs should stop using the product immediately and follow manufacturer recall instructions.
Lannett Company, Inc. recalls 8,544 bottles of Lisdexamfetamine Dimesylate 40 mg capsules distributed nationwide. A labeling mix-up may have placed 30 mg and 40 mg strengths in mislabeled bottles. Healthcare providers and patients should stop use and contact the company for guidance.
Agilent Technologies Denmark ApS recalled 67 FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use antibodies sold nationwide in the United States. The antibody may stain weakly, potentially producing false negative CD20 results. Healthcare facilities should stop using the device immediately and follow manufacturer recall instructions.
Philips Medical Systems Nederland B.V. recalls four IntelliSpace Cardiovascular software units distributed to facilities in Georgia, North Carolina and Texas. A software issue can display outdated information on the device. Hospitals should stop using the device immediately and follow Philips recall instructions.
Glenmark Pharmaceuticals Inc. USA recalls theophylline extended-release 400 mg tablets after dissolution test failures. The recall covers 22,656 bottles distributed nationwide in the United States. Consumers should stop using the product and contact Glenmark for guidance.
Breckenridge Pharmaceutical recalls duloxetine delayed-release capsules due to CGMP deviations raising N-nitroso-duloxetine impurity above interim limit. The bottles were distributed to Arizona, Indiana and New Jersey. Consumers should stop using the product and contact their healthcare provider for guidance.
Baxter Healthcare Corporation issued an urgent medical device recall for one lot of Continu-Flo intravascular solution sets, 14,400 units distributed nationwide in the United States. Customer reports indicate tubing separation. Health care providers and patients should stop using the device immediately and follow recall instructions.
Medline Industries recalled 88 units of the Sterile Extremity Pack DYNJ45701B after finding that kits labeled as sterile had not undergone sterilization. The affected distribution covered Florida, Maryland, New Jersey and Tennessee. Hospitals and clinics should stop using the kit immediately and follow Medline's recall instructions.
Medline Industries, LP recalled 22 sterile convenience kits distributed to Florida, Maryland, New Jersey and Tennessee after determining the kits labeled as sterile had not undergone sterilization. The sterility lapse creates an infection risk for patients. Healthcare facilities and patients should stop using the kits and follow the recall instructions from Medline and the FDA.
Schiller, AG recalls 266 Argus PB-3000 vital sign monitors nationwide in the United States. The devices may display an error message during blood pressure measurements when the initial inflation pressure is set high. Authorities urge users to stop using the device and follow manufacturer instructions.
Glenmark Pharmaceuticals recalls 4,800 bottles of Carvedilol 25 mg tablets distributed nationwide in the USA. The recall cites CGMP deviations and a nitrosamine impurity exceeding the Acceptable Intake Level. Consumers should stop using the product and contact Glenmark or their healthcare provider for guidance.
Glenmark Pharmaceuticals Inc. recalls 6,432 bottles of Carvedilol Tablets, USP, 12.5 mg, distributed nationwide in the United States. The recall concerns CGMP deviations and the presence of a nitrosamine impurity above the acceptable intake level. Consumers should stop taking the product and contact Glenmark for guidance.
Monica Vinader recalls select 14k yellow gold mini heart bracelets, necklaces and stud earrings due to high cadmium levels. The recalled jewelry was manufactured in October and November 2024. Consumers should stop wearing the jewelry immediately and contact Monica Vinader for a replacement or refund.
Glenmark Pharmaceuticals Inc. recalls 44,328 bottles of Carvedilol tablets, 3.125 mg, distributed nationwide in the USA. The impurity N-nitroso carvedilol I exceeds the Acceptable Intake Level. Consumers should stop using the product and contact Glenmark for guidance.
Séfralls Minoxidil Hair Generation Serum, sold by Guangzhou Ariel Biotech, was recalled on August 7, 2025. The serum is packaged in amber dropper bottles with a white and gold dropper and a white, black and gold label. The packaging is not child-resistant, violating the Poison Prevention Packaging Act and creating a poisoning risk for children. Consumers should stop using the serum immediately and
Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition Taurine Mental & Athletic Performance dietary supplement distributed nationwide. The FDA enforcement report cites unapproved drug claims and misbranding. Consumers who purchased this product should not consume it and should contact the company for refund or replacement.
Hi-Tech Pharmaceuticals recalled 85,950 units of Pine Bark Supplements for unapproved drug claims and misbranding. The FDA enforcement notice lists Hi-Tech Pharmaceuticals, Inc. of Norcross, GA as the marketer. The recall cites unapproved drug claims and misbranding as the reason. Consumers should stop using the product and contact the company for refund or replacement information.
Maquet Cardiovascular recalled 98 Vasoview Hemopro 3 EVH systems nationwide across FL, IL, MD and TX after 16 out-of-box failure complaints. No serious injuries were reported. The failures occurred during limited launch before clinical use.