FDASeptember 13, 2017device

14-442000S Antegrade Femoral Nail Instrument Kit, orthopedic instrument

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Fracture of the bolt connecting the insertion guide to the intramedullary nail during insertion of the femoral nail.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
14-442000S Antegrade Femoral Nail Instrument Kit, orthopedic instrument — Recall Details · AllClear