FDAJune 18, 2019device

LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120

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

The hazard

The products' cut, coagulate, or blend function may not operate with the use of the Foot Pedal.

What to do

FDA enforcement status: Terminated

Brands named

coopersurgical

Recall history

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

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