FDAAugust 28, 2017device

Persona Partial Knee System Product Usage: The Persona Partial Knee System instruments are used by a surgeon to facilitate the implantation of PPK implantable components into the medical knee compartment during unicondylar knee replacement.

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

The hazard

Potential for the Persona Partial Knee Impactor Pad to fracture.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

4253990910000880304810242

Recall history

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

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