by Bruce Waldon | Apr 6, 2026 | Alerts, Alerts-Device, Consumer Information, DME, Med-Devices, MedWatch-System, Product Corrections, Safety, US-FDA
FDA Class I Recall Medline homecare beds Home About Consumer News Food and Beverage Supplements Regulatory Medical Devices Pharma Biologics Combination Products Veterinary AI Quality QMSR Central News Enforcement Alerts Innovation Contact Medline Homecare Beds: FDA...
by Bruce Waldon | Mar 23, 2026 | Alerts, Alerts-Device, Industry Information, Industry News, Med-Devices, MedWatch-System, Product Safety, Safety, US-FDA
Medical Device Safety Alert Erbe cryoprobes may rupture or burst Home About Consumer Food and Beverage Supplements Regulatory Medical Devices Pharma Biologics Combination Products Veterinary AI Quality QMSR Central News Enforcement Alerts Innovation Contact FDA Flags...
by Bruce Waldon | Feb 19, 2026 | Alerts-Device, Labeling, Medical Device Labeling, MedWatch-System, Product Corrections
Recall Alert: TRUE METRIX® Blood Glucose Meters Issues with error messaging in labeling Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products Veterinary AI Quality QMSR Central News Enforcement Alerts Innovation Contact Labeling...
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 MDP Staff | Jul 24, 2025 | Alerts, Alerts-Device, Cannula, Cardiovascular, Class I Recalls, Med-Devices, Product Recalls
Recall Alert: Edwards Lifesciences Arterial Cannulae Risk of wire exposure near the cannula tip Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Edwards Lifesciences Arterial CannulaSource: FDA...
by MDP Staff | Jul 24, 2025 | Alerts-Device, Class I Recalls, Med-Devices, Product Recalls
Device Recall: ZOLL AutoPulse NXT Resuscitation System Device may fail to deliver adequate CPR Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Urgent Class I Medical Device Recall ZOLL...
