Reported Nov 13, 2019 · Terminated
Various Knee Systems for knee joint arthroplasty, knee prosthesis, Item Nos. 00522000100 00522000200 00522000300…
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 Knee Systems for knee joint arthroplasty, knee prosthesis, Item Nos.
302 of 302 codes
005220001000052200020000522000300005220004000052200630400522006504005220066000052200680000522006900005220070000052200720000522007300005220074000052200750000522007900005220080000052240080000522400900005224062010054100140100541001501005410015020054100160100541001602005410017010054100170200541001801005410018020054120150100541201502005412016010054120160200541201701005412017020054120180100541201802005414013010054140130200541401401005414014020054140150100541401502005414016010054140160200541401701005414017020054160140100541601402005416015010054160150200541601601005416016020057500130100575001302005750013050057500130600575001401005750014020057500140500575001406
- 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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