FDAApril 26, 2023device

MRI Biomet Pin Guide for Total Knee Arthroplasty (Zimmer Biomet Patient Specific Instruments (PSI)-- patient-matched device designed to fit the patients anatomy to transfer a patient-specific pre-operative plan to the OR. Ref: KNM-ZB02-00-01

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

The hazard

The wrong tibia guide was included intended for a different patient case.

What to do

FDA enforcement status: Completed

Brands named

materialise n vmaterialise

UPCs

05420060310027

Recall history

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

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