FDA recall Z-0773-2018

Zimmer Biomet, Inc. · Class II · device

Product

Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa, Model#14-442093 Antegrade Femoral Connecting Bolt. 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-0773-2018