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Biomet, Inc. recalls REF 200068 Security (TM) Enclosed Carpal Tunnel System Blade ( Single) ABS /Stainless Steel Sterile Device, Single Us
Recalled December 4, 2013 · FDA recall Z-0381-2014 · Biomet
Hazard
Security Blades were manufactured oversized and potentially won't advance or may be difficult to advance through the mating Security Clip. · FDA Class II
Units
1130
Sold at
Worldwide Distribution: USA (nationwide) and Internationally to Japan.
Description
Security Blades were manufactured oversized and potentially won't advance or may be difficult to advance through the mating Security Clip.
Product
REF 200068 Security (TM) Enclosed Carpal Tunnel System Blade ( Single) ABS /Stainless Steel Sterile Device, Single Use Only. Designed to release the transverse carpal ligament.
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →