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FDAOctober 24, 2017device

Persona Partial Knee Spacer Blocks To assist in partial knee arthroplasty surgery

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

The hazard

Zimmer Biomet is conducting a medical device recall for the Persona Partial Knee Spacer Blocks in sizes 8mm, 9mm, 10mm, 12mm, and 14mm. Complaints received indicated that flexion has the potential to feel tight during range-of-motion trialing and that the final trial has the potential to appear looser in extension.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

42539903508

Recall history

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

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