16,499 Physio-Control Infant/Child Defibrillator Electrodes Recalled for Delamination Risk
Due to pediatric defibrillator electrode delamination
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Due to pediatric defibrillator electrode delamination
Stryker recalled 5,864 units of the MOLLI 2 surgical markers on January 21, 2026. The recall follows concerns that magnetic surgical tools may dislodge markers during procedures. Healthcare providers and patients must stop using these devices immediately.
Unichem Pharmaceuticals recalled 60,000 bottles of Doxazosin Tablets on January 21, 2026. The tablets were imprinted with the wrong ID, posing a serious risk to consumers. Healthcare providers and users should stop using the product immediately.
Nationwide recall of Dukal BZK Antiseptic Towelettes due to CGMP deviations. The products are manufactured for Dukal, LLC in Ronkonkoma, NY and distributed across the United States. Stop using immediately and contact ACME United Corporation for guidance.
ACME United Corporation recalled 212,607,900 First Aid Only BZK Antiseptic Towelettes sold nationwide. The recall cites CGMP deviations in manufacturing. Consumers should stop using the product immediately and contact ACME United Corporation for guidance.
Receive immediate notifications when medications you care about are recalled. Stay safe with timely FDA drug safety alerts.