Reported Nov 13, 2019 · Terminated
Periarticular locking plate elbow-sterile, Item Nos. 47235800503 47235800509 47235800511 47235800515 47235800519…
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?
- Periarticular locking plate elbow-sterile, Item Nos.
47235800503472358005094723580051147235800515472358005194723580060347235800605472358006074723580060947235800611472358006154723580061947235800705472358007114723580071547235800803472358008054723580080747235800811472358008154723580091147235800913472358009154723580120947235801211472358012134723580121547235802305472358023074723580231147235802315472358024054723580240747235802409472358024114723580241547235810707472358107114723581071547235810805472358108074723581081147235810815
- 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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