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FDASeptember 7, 2017device

The 2nd Assist Knee Positioner

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

The hazard

Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

Recall history

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

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