Dräger’s Breathing System Filter Recall Gets Class I Label from FDA After Ventilation Obstruction
Dräeger Medical, Inc. expanded on its voluntary recall of Lot LT2103 of Draeger SafeStar 55 Breathing System Filters.
Read More
Search Results for: recall
GE Healthcare’s Recall of Ventilator Batteries Gets Class I Label from FDA Over Device Shutdown Risk
Due to their ability to cause the premature shutdown of GE Healthcare’s Carescape R860 ICU ventilators, the U.S. FDA has deemed GE Healthcare’s recall of more than 100,000 batteries as a Class 1 event—the most severe kind.
Read More
Medtronic’s HVAD Pump Implant Kit Gets Class I Recall for Weld Defect
Medtronic recalled its HeartWare Ventricular Assist Device System, which is designed to help the heart pump blood to the rest of the body.
Read More
Ordr to Highlight Security Best Practices at AAMI eXchange
Ordr is presenting with The Mayo Clinic & El Camino Health to discuss best practices to secure healthcare organizations at AAMI eXchange 2022.
Read More
Abbott Recalls Imaging Catheter for Potential Loose Catheter Marker Band
The U.S. FDA has identified the Dragonfly OpStar imaging catheter as a Class I recall, the most serious type of recall.
Read More