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...
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 | Mar 14, 2025 | Alerts, Alerts-Pharma, Class I Recalls, Product Recalls
Class I Recall: Dr Reddy's Levetiracetam Injection Mislabeling creates threat of incorrect dosing Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact What You Need to Know Dr. Reddy’s Laboratories...
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 ...
