Reported Jul 22, 2015 · Terminated
ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.
Zimmer, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Zimmer, Inc. · 1800 W Center St · Warsaw, IN · 46580-2304
Is this the product you have?
- ZNN Antegrade Femoral Nail (ZNN AF). Orthopedic internal fixation device.
- Lot codes and dates
Part 47-2492-320-10lot 62763724
- Amount recalled
- 8
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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