Medical Device Recalls Linked to Failure To Enforce Post-Approval Trials
Diagnostic Computer Recalled Due to Calculating Error
Wire Placement Problem Prompts Recall of Grounding Pads
Compromised Sterility Leads To Recall of Dressing
Disposable Syringe Kits Subject of Recall
Firm Recalls Drill Guide Kit
Power Burs Recalled Due to Questionable Sterility
Moisture Leads to Cochlear Stimulator Recall
Needlestick Prevention : Where Are the Device-Specific Data?
Nursing Home Patient Severely Scalded
Hospitals Mistakenly Clean Surgical Tools With Hydraulic Oil
Floor Buffer Rockets Into MRI Machine
Remote Control to a Brain Implant Stolen
FDA Issues Guidance on Networked Device Cybersecurity
Yale-New Haven Hospital Installs Automated IV Filler
Philips Wins Coveted No. 1 Ranking in Customer Service Survey
FDA Reclassifies Series of Devices to a Less-Stringent Marketing Approval Process