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FDAJanuary 25, 2017device

The UNI-CP System; Model Number: 330230SND.

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

The hazard

The firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP plate was incorrect.

What to do

FDA enforcement status: Terminated

Brands named

integra lifesciencesintegra

Recall history

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

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