Reported Nov 13, 2019 · Terminated
Various Devices for Limb salvage arthroplasty, Item Nos. 00585000011 00585001201 00585001202 00585001301 00585001302…
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 Devices for Limb salvage arthroplasty, Item Nos.
93 of 93 codes
005850000110058500120100585001202005850013010058500130200585003038005850032140058500321700585003219005850032380058500324600585004445005850044550058500446500585004603005850046040058500460500585004606005850046080058500461000585004612005850046140058500461600585004618005850046200058500462200585004635005850046450058500465500585004808005850048090058500482000585204209005852042170058520500900585205010005852050110058520501200585205013005852050140058520501500585205016005852050170058520501800585205019005852052090058520521000585205211005852052120058520521300585205214005852052150058520521600585205217005852052180058520521900585205412005852054130058520541400585205415
- 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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