FDAJanuary 27, 2020device

Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented total knee prosthesis system, which provides femoral components, tibial inserts, stems, augments, and surgical instrumentation for use in primary and revision total knee arthroplasty.

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

The hazard

These Truliant Splined Stem Extension, 18mm x 120mm were found to have a labeling error. The upper right corner of the label incorrectly identifies the implant size as 17mm x 80mm when the implant size is 18mm x 120mm.

What to do

FDA enforcement status: Ongoing

Brands named

exactech

UPCs

02012641812

Recall history

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

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Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented total knee prosthesis system, which provides femoral components, tibial inserts, stems, augments, and surgical instrumentation for use in primary and revision total knee arthroplasty. — Recall Details · AllClear