FDAMay 18, 2018device

Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 141215; UDI: (01) 00880304005310 (17) 280306 (10) 385340 Product is used in Total Knee Arthroplasty

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

The hazard

One lot of 75mm tibial tray is potentially etched and labeled as a 79 mm tibial tray. This may lead to delay in surgery, or immediate revision surgery to remove an incorrectly sized tibial component after it has been cemented.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

00880304005310

Recall history

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

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