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FDAFebruary 28, 2017device

Xl por st 24.0x220mm, bowed, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

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

The hazard

Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

00992124033

Recall history

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

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Xl por st 24.0x220mm, bowed, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants — Recall Details · AllClear