Health & Personal Care
HIGH
FDA DEVICE
Changchun Wancheng Bio-Electron Recalls Vivoo pH Test for Inaccurate Results
Changchun Wancheng Bio-Electron Co.
Test strips
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Health & Personal Care
HIGH
FDA DEVICE
Changchun Wancheng Recalls Male Fertility Test Over False Results
Changchun Wancheng Bio-Electron Co. recalled 1,000 male fertility sperm tests on November 22, 2025. The tests were distributed without proper FDA clearance and may yield inaccurate results. This could lead to inappropriate medical interventions by users.
Changchun Wancheng Bio-Electron Co.
Test strips
Health & Personal Care
HIGH
FDA DEVICE
Vivoo Vaginal pH Test Recalled Over Inaccurate Results Risk
Vivoo recalled 3,000 vaginal pH tests on November 22, 2025. The tests may cause false results leading to inappropriate medical interventions. The products were distributed nationwide, including Texas, Georgia, and California.
Changchun Wancheng Bio-Electron Co.
Test strips
Health & Personal Care
HIGH
FDA DEVICE
Changchun Wancheng Recalls Male Fertility Test Over Inaccurate Results
Changchun Wancheng Bio-Electron Co.
Test strips
Health & Personal Care
HIGH
FDA DEVICE
Changchun Wancheng Recalls Ovulation Test Over False Results Risk
Changchun Wancheng Bio-Electron Co.
Test strips
Health & Personal Care
HIGH
FDA DEVICE
Dr. Anna Cabeca Test Strips Recalled Over False Diagnostic Risks
Changchun Wancheng Bio-Electron Co.
Test strips
Health & Personal Care
HIGH
FDA DEVICE
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 Co.
Test strips
Health & Personal Care
HIGH
FDA DEVICE
LotFancy Urinary Tract Infection Test Strips Recalled for False Results
Changchun Wancheng Bio-Electron Co.
Test strips
Health & Personal Care
HIGH
FDA DEVICE
Changchun Wancheng Bio-Electron Recalls Vivoo Protein Test Over False Results
Changchun Wancheng Bio-Electron Co.
Test strips
Health & Personal Care
HIGH
FDA DEVICE
Changchun Wancheng Bio-Electron Recalls Menopause Test Cassette
Changchun Wancheng Bio-Electron Co.
Test strips
Health & Personal Care
HIGH
FDA DEVICE
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.
Roche Diagnostics Operations
Issues identified:
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls Oxygen Masks Due to Tubing Disconnect Risk
Medline Industries, LP
Firm received
Health & Personal Care
HIGH
FDA DRUG
Glenmark Pharmaceuticals Recalls Bisoprolol Tablets Due to Contamination
Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe
BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE
Cross Contamination
Health & Personal Care
HIGH
FDA DEVICE
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.
Fresenius Kabi USA
Emphasizing instructions
Health & Personal Care
HIGH
FDA DEVICE
CareFusion 303 Recalls Automated Dispensing Cabinets Due to Error Risk
CareFusion 303
Automated Dispensing
Health & Personal Care
HIGH
FDA FOOD
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
A New Life Herbs
Unapproved drug
Health & Personal Care
HIGH
FDA DEVICE
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.
Medtronic Neuromodulation
Software issue
Health & Personal Care
HIGH
FDA FOOD
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
Unapproved drug
Health & Personal Care
HIGH
FDA FOOD
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
Unapproved drug
Health & Personal Care
HIGH
FDA FOOD
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
Unapproved drug
Health & Personal Care
HIGH
FDA DRUG
Fagron Compounding Services Recalls Ophthalmic Solution Over Incorrect Formulation
Fagron Compounding Services
Incorrect Product
Health & Personal Care
HIGH
FDA FOOD
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
Unapproved drug
Health & Personal Care
HIGH
FDA DEVICE
Vortex Surgical Recalls Laser Probe Due to Smooth Passage Issues
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Vortex Surgical
Reason for
Health & Personal Care
HIGH
FDA DEVICE
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.
Steris
Wire connected
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