FDA Investigates Root Causes of Surgical Stapler Adverse Events
Patient Injuries Cited in Hygiene Chair Recall
Coronary Stents Recalled Due to Slow Balloon Deflation
FDA Corrections
Firm Completes Recall of Pulse Oximetry Software
Scissoring Leads to Recall of Clip Appliers
Devices Recalled; Overheating, Melting Potential Cited
Firm Completes Recall of Software
Defibrillators Recalled; Standards Not Met
Recall of Cranial Access Kit Complete
Software Recalled; Possible System Crash Cited
Implantable Pulse Generators Recalled
Anesthesia Products Recalled; Lidocaine Cited
Sterility Concern Leads to Recall of Balloon Catheter
Lack of Latex Label Prompts Product Recall
Safety IV Catheters Recalled; Mislabeling Blamed
Image Navigator Software Feature Recalled
Three Years of Mammographies Performed at Florida Center Could Be Flawed
“Da Vinci” Surgical Robot Cleared for Heart Surgery