by Bruce Waldon | Apr 10, 2026 | Alerts, Alerts-Device, Class I Recalls, FDA Safety Communication, MedWatch-System, Product Recalls, US-FDA
FDA Early Alert Cook Medical sizing catheters Home About Consumer News Food and Beverage Supplements Regulatory Medical Devices Pharma Biologics Combination Products In Vitro Diagnostics Veterinary AI Quality QMSR Central News Enforcement Alerts Innovation Contact...
by Bruce Waldon | Mar 15, 2026 | Consumer Information, Consumer Safety, Dietary Supplements, Editorial, FDA Safety Communication, Industry Information, Labeling, Safety, Unapproved Drugs, US-FDA
Honey-Based Dietary Supplements Recalled Sildenafil and tadalafil not declared on product labeling Home About Consumer Food and Beverage Supplements Regulatory Medical Devices Pharma Biologics Combination Products Veterinary AI Quality QMSR Central News Enforcement...
by Bruce Waldon | Mar 15, 2026 | Alerts, Alerts-Supplements, Dietary Supplements, FDA Safety Communication, Industry Information, Industry News, Product Recalls, US-FDA
Recall Alert: Honey-Based Dietary Supplements Contained drugs not declared on product labeling Home About Consumer Food and Beverage Supplements Regulatory Medical Devices Pharma Biologics Combination Products Veterinary AI Quality QMSR Central News Enforcement Alerts...
by MDP Staff | Jul 25, 2025 | Alerts, Alerts-Device, Class I Recalls, FDA Safety Communication, Industry News, Med-Devices, Product Recalls, Product Safety, Safety, Surgical
Ethicon Issues Safety Alert for Endopath Echelon Vascular Reload Surgical Stapler Cartridge Correction Home About Consumer Medical Devices Pharma Biologics Biologics Warning Letters AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Endopath...
by Devices and Pharma | Jul 10, 2025 | Alerts-Device, Class I Recalls, FDA Safety Communication, Industry News, Med-Devices, MedWatch-System, Product Recalls, US-FDA
Avanos Recalls Ballard Closed Suction Systems Due to sterilization failure Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact May result in non-sterile devices Avanos Medical, Inc. is recalling its...
by Devices and Pharma | Jul 8, 2025 | Alerts-Device, Class I Recalls, FDA Safety Communication, Med-Devices, MedWatch-System, Product Recalls, Product Safety
FDA Alert: Abiomed Impella Blood Pump Urgent Recall Controller may fail to detect the Impella device Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Abiomed Impella blood pump controllers...
