Reported Mar 7, 2018 · Terminated
979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument.
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. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
- 979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument.
- Lot codes and dates
- Finished Lot order
M370490M354450M321540M975460M639280M426760M629950M629930M073530M073540M073550M073560M073570M073580M073590M073600M073610M627490M656470M656580M656590M656600M656610M656620M656640M656660M966880M967050M967060M967070M980260M980270M508490M508410M508500M508450M508480M508520M508470M508510M508460
- Finished Lot order
- Amount recalled
- 337 total
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
Why it was recalled
Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
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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