Reported Nov 13, 2019 · Terminated
Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate Item Nos. 47235700306 47235700308 47235700310 47235700312…
Zimmer 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: Zimmer Biomet, Inc. · 1800 W Center St · Warsaw, IN · 46580-2304
Is this the product you have?
- Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate Item Nos.
4723570030647235700308472357003104723570031247235700314472357004084723570041047235700412472357004144723570041647235700504472357005064723570050847235700510472357005124723570051447235700518472357006044723570060647235700608472357006104723570061247235700614472357006184723570070647235700708472357007104723570071447235700808472357008104723570081447235700906472357009084723570091447235700918472357010064723570100847235701010
- Lot codes and dates
- All product manufactured prior to January 2014.
- Amount recalled
- 5,459,583 total devices
This recall covers 41 products
The agency filed one notice per product. You are reading one of them; the other 40 are below.
28 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
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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