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...
by MDP Staff | Jul 16, 2025 | Alerts, Alerts-Device, Class I Recalls, Product Recalls, Product Safety, Safety
Cranial Drill Urgent Recall Alert Serious safety risks Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Urgent Class I Medical Device Recall Integra LifeSciences has issued an urgent recall of...
by MDP Staff | Jul 15, 2025 | Alerts, Alerts-Device, Class I Recalls, FDA Reports
BD Alaris Pump Module model 8100 Performance can worsen when connected to other perfusion sets Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Class I Recall (Correction) The FDA has issued an...
by Devices and Pharma | Jul 10, 2025 | Alerts-Device, Class I Recalls, Med-Devices, MedWatch-System, Product Recalls, Products_Devices, Safety, US-FDA
AirLife/Vyaire Infant Breathing Systems Recall Potential for risk of disconnection Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Class I Recall AirLife and manufacturer Vyaire are recalling...
