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FDAApril 28, 2017device

VERSA-FXII SC TUBE PLT 90DX16H, 95DX16H, 95DX18H, 95DX20H, 95DX22H

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

The hazard

Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

0011930901600119309516001193095180011930952000119309522

Recall history

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

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