Reported Dec 17, 2014 · Terminated
Total Temporomandibular Joint Replacement System- 50mm Lft Standard Ti Mandi Reconstruction of the temporomandibular…
Biomet Microfixation, LLC
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 Microfixation, LLC · 1520 Tradeport Dr · Jacksonville, FL · 32218-2480
Is this the product you have?
- Total Temporomandibular Joint Replacement System- 50mm Lft Standard Ti Mandi Reconstruction of the temporomandibular joint
- Lot codes and dates
Model 24-6551TILot #s: 544160A525190A525190B525180B544170A544180B544160B525180A544180A
- Amount recalled
- 42
This recall covers 14 products
The agency filed one notice per product. You are reading one of them; the other 13 are below.
1 more are in the archive.
Where it was sold
Why it was recalled
Laser etching on the parts is wider and deeper than the conditions previously validated.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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