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Device Recall Alert: Edwards Lifesciences Arterial Cannula

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...

Device Recall: ZOLL AutoPulse NXT Resuscitation System

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...

Urgent Recall of Codman Disposable Perforators

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...

What Are Early Recall Alerts?

by MDP Staff | Jul 15, 2025 | Alerts, Alerts-Device, FDA_Innovation, Product Recalls, US-FDA

FDA Pilot Program Updates Recall Reporting The goal is to improve early communication Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Recall Communication “Early Alerts” Note: This summary is...

Urgent Recall Alert for BD Alaris Infusion Sets

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...

Recall Alert: AirLife/Vyaire Infant Breathing Systems

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...
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