Reported Nov 13, 2019 · Terminated
Periarticular Plates - Tibial, Item Nos. 00234700304 00234700306 00234700308 00234700310 00234700312 00234700314…
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?
- Periarticular Plates - Tibial, Item Nos.
80 of 80 codes
002347003040023470030600234700308002347003100023470031200234700314002347003160023470040400234700406002347004080023470041000234700412002347004140023470041600234700502002347005040023470050600234700508002347005100023470051200234700514002347006020023470060400234700606002347006080023470061000234700612002347006140023470070400234700706002347007080023470071000234700712002347007140023470071600234700718002347007200023470080400234700806002347008080023470081000234700812002347008140023470081600234700818002347008200023470090400234700906002347009080023470091000234700912002347009140023470091600234700918002347009200023470100400234701006002347010080023470101000234701012
- 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.
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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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