Health & Personal Care Recalls

Changchun Wancheng Recalls Male Fertility Test Over Inaccurate Results

LotFancy Urinary Tract Infection Test Strips Recalled for False Results

Changchun Wancheng Bio-Electron Recalls Menopause Test Cassette

Dr. Anna Cabeca Test Strips Recalled Over False Diagnostic Risks

Changchun Wancheng Bio-Electron Recalls Diagnostic Test Strips

Changchun Wancheng Bio-Electron Co. recalled 1,000 units of S. Typhi/Para Typhi A Antigen test strips on November 22, 2025. The recall affects tests distributed nationwide, which may produce false results and lead to inappropriate medical intervention.

Changchun Wancheng Bio-Electron Recalls Vivoo Protein Test Over False Results

Medline Recalls Oxygen Masks Due to Tubing Disconnect Risk

Glenmark Pharmaceuticals Recalls Bisoprolol Tablets Due to Contamination

Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe

Fresenius Kabi Recalls Ivenix Infusion System Software Over Safety Issues

Fresenius Kabi USA recalled 30 units of the Ivenix Infusion System LVP Software on November 21, 2025. The recall addresses concerns related to programming instructions for LVP duration. Patients and healthcare providers must stop using the device immediately.

Roche Diagnostics Recalling Anti-TSHR Immunoassay Over Diagnosis Risk

Roche Diagnostics Operations recalled 1,300 Anti-TSHR immunoassay cassettes on November 21, 2025. Variability in results may lead to incorrect diagnoses and treatment delays. The recall affects multiple states across the U.S.

Fagron Compounding Services Recalls Ophthalmic Solution Over Incorrect Formulation

CareFusion 303 Recalls Automated Dispensing Cabinets Due to Error Risk

A New Life Herbs Recalls Ear Drops Over Misbranding Issues

A New Life Herbs, LLC recalled 22 bottles of Mullein flower alcohol tincture on November 20, 2025. The product is misbranded due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using this product immediately.

A New Life Herbs Recalls Sinus Cap Herbal Supplement Over Misbranding

A New Life Herbs recalled Sinus Cap Herbal Supplement on November 20, 2025, due to unapproved drug claims. The product lacks a Supplement Facts label, which misbrands it. Consumers should not consume the product and seek refunds or replacements.

A New Life Herbs Recalls Baby Soothe Herbal Supplement Over Misbranding

A New Life Herbs recalled 49 bottles of Baby Soothe Herbal Supplement on November 20, 2025. The product misbrands due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using the product immediately and seek a refund.

A New Life Herbs Recalls Boswellia Herbal Supplement Over Labeling Issues

A New Life Herbs, LLC recalled 278 bottles of Boswellia Herbal Supplement on November 20, 2025. The product has unapproved drug claims and lacks a Supplement Facts label. Consumers should stop using it immediately and seek a refund.

A New Life Herbs Recalls Baby Allergy Herbal Supplement Over Label Issues

Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

Medtronic Recalls Clinician Programmer App Over High-Risk Software Issue

Medtronic Neuromodulation recalled 7,667 Clinician Programmer Applications on November 20, 2025. A software issue may prevent patients from resuming therapy, leading to a recurrence of pain symptoms. Affected models include A71100 and associated tablets.

Steris Washers Recalled Due to Electrical Arcing Hazard

Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).

Steris Recalls AMSCO 7052HP Washer/Disinfector Due to Fire Hazard

Steris recalled the AMSCO 7052HP Washer/Disinfector on November 19, 2025, after reports of electrical arcing. The issue results from a wire potentially shifting out of position, posing a fire risk. No injuries or shocks have been reported.