Acid-Reflux Surgical Device Under Investigation
Class I Recall of Analyzers Complete
Class I Recall of Coronary Stent Systems Begun
Devices with Introducer Tubing Recalled
Battery Pack Recalled; Lead Wire Not Connected
Skull Pins Recalled; Fracture Below Specifications
Mislabeling Leads to Stent Recall
Generator Failure Leads to Recall
Hip Stem Recall Complete
Heat, Moisture Exchangers Recalled, Sterility Cited
Firm Finds Holes in Packaging, Recalls Cords
Catheter Recalled; Separated from Hub
Firm Recalls Staple Remover Kits
Recall of Temperature Regulation System Complete
Sterility Concern Leads to Recall of Glass Cartridges
Medical Errors May Claim Far More Lives Than Predicted
FDA Seeks Injunction Against Utah Medical Device Manufacturer
Rudy the Robot Takes Telemedicine to the Next Level