Reported Dec 4, 2013 · Terminated
REF 200068 Security (TM) Enclosed Carpal Tunnel System Blade ( Single) ABS /Stainless Steel Sterile Device, Single Use…
Biomet, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
- 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.
- Lot codes and dates
- Catalog Number200068
- Medical Device Listing NumberB008657
- Lot Number Identification
088610090600143810257060289900365910460490558300626660697320767260795090857730864640979680
- Amount recalled
- 1130
Where it was sold
- Nationwide
Why it was recalled
Security Blades were manufactured oversized and potentially won't advance or may be difficult to advance through the mating Security Clip.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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