Reported Nov 13, 2019 · Terminated
Various fixation systems and accessories, Item Nos. 00224000916 00224000918 00224000920 00224000922 00224000924…
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?
- Various fixation systems and accessories, Item Nos.
304 of 304 codes
002240009160022400091800224000920002240009220022400092400224000926002240009280022400093000224000932002240009340022400093600224000938002240009400022400094200224000944002240009460022400101400224001016002240010180022400102000224001022002240010240022400102600224001028002240010300022400103200224001034002240010360022400103800224001040002240010420022400104600224001048002240011140022400111600224001118002240011200022400112200224001124002240011260022400112800224001130002240011320022400113400224001136002240011380022400114000224001142002240011440022400114600224001214002240012160022400121800224001220002240012220022400122400224001226002240012280022400123000224001232
- Lot codes and dates
- All products 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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