Reported Nov 13, 2019 · Terminated
Various Hip Joint Replacement Systems, Item Nos. 00151504232 00151504432 00151504636 00151504836 00151505040…
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 Hip Joint Replacement Systems, Item Nos.
304 of 304 codes
001515042320015150443200151504636001515048360015150504000151505240001515054440015150564400151505848001515060480015150624800151506448001515066480040050006000401000038004010000400040100004100401000042004010000430040100004400401000045004010000460040100004700401000048004010000490040100005000401000051004010000520040100005300401000054004010000550040210085700402100863004021012430040210124400402200040004022000420040220005100402200057004088011060040880120600408801226004088012360040880130600408801326004088013360040880135600408801376004088014060040880142600408801436004088014560040880147600408801506004088015260040880153600408801556004088015760040880160600408801626
- 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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