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FDAApril 28, 2017device

VERSA-FX II STD TUBE 130DX16H, 130DX18H, 130DX20H, 135DX16H, 135DX18H, 135DX20H, 140DX16H, 140DX18H, 140DX20H, 145DX16H, 145DX18H, 145DX20H, 150DX16H, 150DX18H, 150DX20H

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

001193130160011931301800119313020001193135160011931351800119313520001193140160011931401800119314020001193145160011931451800119314520

Recall history

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

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