FDANovember 7, 2019device

Ligamax 5 mm Endoscopic Multiple Clip Applier

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

The hazard

A potential exists that certain LIGAMAX devices within the impacted lots may have small holes in the Tyvek lidding which could result in a breach of sterility.

What to do

FDA enforcement status: Terminated

Brands named

ethicon endo surgeryethiconethicon endo

Recall history

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

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