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...
by Devices and Pharma | Apr 28, 2024 | Alerts, Alerts-Device, Class I Recalls, Consumer Information, Med-Devices, MedWatch-System, Product Recalls, Product Safety
DeRoyal Industries, Inc. recalls Tracecarts under recall by Nurse Assist Contents include 16FR Urine Meter Foley catheter Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation...
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 17, 2024 | Alerts, Alerts-Device, Class I Recalls, Med-Devices, MedWatch-System, Product Recalls
Urgent Recall Notice for Boston Scientific Obsidio Conformable Embolic Increased bowel ischemia risk with lower GI bleeding Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation...
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...
by Devices and Pharma | Apr 3, 2024 | Alerts, Alerts-Device, Class I Recalls, Consumer Safety, FDA Safety Communication, Med-Devices, MedWatch-System, Product Recalls, Product Safety, US-FDA
Urgent recall notice for the ARROW QuickFlash Line Catheterization Kits Increased risk of damage to blood vessel walls, vasospasm, artery blockage Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News...
