Reported Oct 28, 2015 · Terminated
Thinflap System Case The cases hold surgical instrumentation in place during handling and storage.
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?
- Thinflap System Case The cases hold surgical instrumentation in place during handling and storage.
- Lot codes and dates
- Lot Code # 101465 Model # 19-5000
- Amount recalled
- 5 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
The lids on implant caddies within P/N 17-5000 and 19-5000 could not be opened by the user without application of undesirable/unexpected excessive force.
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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