FDAJanuary 25, 2023device

TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product label/labeling)

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

The hazard

Due to the incorrect component, that is not cleared to be marketed in the U.S., being included in its elbow prosthesis.

What to do

FDA enforcement status: Ongoing

Brands named

limacorporate s p alimacorporate

UPCs

08033390128865

Recall history

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

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