FDA Issues Stern Letter of Warning to Boston Scientific
Fraying, Tearing Leads to Class I Graft Recall
Recall of OneTouch Owner's Booklet Complete
Lock Box for Pump Family Recalled
Biliary Stents Recalled
Recall of Fascial Dilator Complete
Compromised Sterility Prompts Pouch Recall
Infusion Pump Recalled; Assembly May Detach
Possible Breakage Leads to Recall of Surgical Instrument
Recall of Therapy Bed Complete
Dilation Catheter Recalled; Wire Movement Difficulty Cited
Possible Fluid Leak Prompts Recall of Pressure Monitor Kit
Incorrect Markings Lead to Recall of Shoulder Prosthesis
Patient Monitor Network Software Recalled
Unsealed Packages Prompt Probe Cover Recall
Leaky Valves Lead to Sheath Recall
Correction