by Devices and Pharma | Apr 27, 2024 | Alerts, Alerts-Device, Class I Recalls, Consumer Safety, Industry News, Med-Devices, Product Recalls, Product Safety, US-FDA
Fresenius Medical Care Recalls Stay-Safe Catheter Extension Sets and Stay-Safe Adapter High risk of exposure to toxic compound NDL-PCBA Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts...
by Devices and Pharma | Apr 21, 2024 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, MedWatch-System, Product Recalls, Product Safety, US-FDA
Abbott/Thoratec Corp. Recalls HeartMate II and HeartMate 3 Biological material buildup may obstruct flow Home About Consumer Medical Devices Pharma AI Regulatory Quality News Enforcement Alerts Innovation Contact Recall Alert: HeartMate II and HeartMate 3 Left...
by Devices and Pharma | Apr 18, 2024 | FDA Reports, Industry News, Med-Devices, Product Safety, US-FDA
CDRH Issues its 2024 Safety Report Commitment to safety and effectiveness of medical devices Home About Consumer Medical Devices Pharma Biologics Biologics Warning Letters AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact 2024 CDRH Safety...
by Devices and Pharma | Apr 17, 2024 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, Product Recalls, Product Safety
Fresenius Kabi Recalls Ivenix Infusion Pump Software Software anamolies could cause patient harm and fatalities Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact...
by Devices and Pharma | Apr 17, 2024 | Alerts, Alerts-Device, Class I Recalls, Consumer Safety, Med-Devices, Product Recalls, Product Safety
Medos International Recalls CEREBASE DA Guide Sheath Due to cracking of its distal catheter shaft Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact Urgent Class I...
by Devices and Pharma | Apr 15, 2024 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, MedWatch-System, Product Recalls, Product Safety
Datex-Ohmeda Issues Field Correction for EVair Air Compressors Formaldehyde emissions when used with certain ventilators Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation...
