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...
by Devices and Pharma | Jul 7, 2025 | Alerts-Device, Class I Recalls, FDA Safety Communication, Industry News, Product Recalls, Products_Devices
GE HealthCare Anesthesia Systems Recall potentially life-threatening risk in Volume Control Ventilation (VCV) mode Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact GE Carestation Anesthesia...
by Devices and Pharma | Jul 4, 2025 | Alerts, Alerts-Device, Class I Recalls, Industry News, Med-Devices, MedWatch-System, Product Recalls, Product Safety
FDA Alert: Baxter Recalls Spectrum Infusion Pumps Software error could result in dangerous dosing Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Baxter Spectrum Infusion Pump Alert Date: July...
by Devices and Pharma | May 2, 2024 | Alerts, Alerts-Device, Consumer Information, Consumer Safety, FDA Safety Communication, Industry Information, Industry News, Med-Devices, Product Safety, US-FDA
FDA Safety Communication - Exactech Equinoxe Shoulder System Potential risks with products packaged in defective bag Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact FDA Safety Communication April 19...
by Devices and Pharma | Apr 30, 2024 | Alerts, Alerts-Device, Class I Recalls, Industry News, Med-Devices, Pharmaceuticals, Product Recalls
Recall Notice for BioMérieux VITEK 2 AST Kit An anomaly in Ceftriaxone concentrations results in misreading bacterial susceptibility Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact Class I Recall Notice ...
by Devices and Pharma | Apr 29, 2024 | Alerts-Device, Class I Recalls, Industry News, Med-Devices, MedWatch-System, Product Recalls, Product Safety, US-FDA
SonarMed Inc. Recalls Airway Acoustic Sensors Restriction of inner diameter may impede catheter passage Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact Urgent Class I Recall Notice SonarMed Inc. has issued...
