FDA recall Z-0774-2018

Zimmer Biomet, Inc. · Class II · device

Product

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.

Distribution

Distribution includes US Nationwide.

Key facts

Status: Terminated
Initiation date: 2017-09-13
Report date: 2018-03-07
Termination date: 2020-04-21
Voluntary/Mandated: Voluntary: Firm initiated
Location: Warsaw, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0774-2018