Reported Nov 13, 2019 · Terminated
ZPLP Fibular Plate, Item Nos. 00234701504 00234701506 00234701508 00234701510 00234701512 00234701516 00234701604…
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?
- ZPLP Fibular Plate, Item Nos.
002347015040023470150600234701508002347015100023470151200234701516002347016040023470160600234701608002347016100023470161200234701614002347016160023470170200234701704002347017060023470170800234701710002347017120023470171400234701716002347017180023470180200234701804002347018060023470180800234701810002347018120023470181400234701816002347018184723570170447235701706472357017084723570171047235701712472357017144723570171647235701804472357018064723570180847235701810472357018124723570181447235701816
- 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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