FDAJune 17, 2015device

ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.

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

The hazard

A single distributed ZNN Greater Trochanter Femoral Nail may have been dented. Potential for fatigue of implant prior to sufficient fracture healing, which may result in need for implant removal and revision of fracture fixation to assure proper healing and avoid fracture malunion or nonunion.

What to do

FDA enforcement status: Terminated

Brands named

zimmer

UPCs

47249232010

Recall history

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

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