Reported Nov 13, 2019 · Terminated
Various Knee Systems, Item Nos. 32855411838 32855411840 32855411842 32855411843 32855420307 32855420308 32855420309…
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, Item Nos.
186 of 186 codes
328554118383285541184032855411842328554118433285542030732855420308328554203093285542031032855420315328554304913285543049732855430499328554305003285543050232855430503328554305113285543052632855430530328554305313285543053632855430537328554305383285543053932855430541328554305433285543054632855430548328554305493285543055032855430551328554305563285543055732855430558328554305633285543056532855430567328554305683285543056932855430570328554305743285543057532855430577328554504203285545044132855450453328554504613285545049932855470626328554706393285547064132855470644328554706453285547064832855470649328554706523285547065332855470654328554706603285547066332855470666
- 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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