14-442000S Antegrade Femoral Nail Instrument Kit, orthopedic instrument
Reported: March 7, 2018 Initiated: September 13, 2017 #Z-0774-2018
Product Description
14-442000S Antegrade Femoral Nail Instrument Kit, 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? ▼
14-442000S Antegrade Femoral Nail Instrument Kit, 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-0774-2018.
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