979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument.
Reported: March 7, 2018 Initiated: September 13, 2017 #Z-0775-2018
Product Description
979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument.
Reason for Recall
Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
Details
- Recalling Firm
- Zimmer Biomet, Inc.
- Units Affected
- 337 total
- Distribution
- Distribution includes US Nationwide.
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument.. Recalled by Zimmer Biomet, Inc.. Units affected: 337 total.
Why was this product recalled? ▼
Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 7, 2018. Severity: Moderate. Recall number: Z-0775-2018.
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