FDAApril 1, 2016device

Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general surgical procedures. Distributed individually and in kits.

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

The hazard

Increased customer complaints indicating inconsistent clip application; may lead to unoccluded vessels.

What to do

FDA enforcement status: Terminated

Brands named

applied medical resourcesappliedapplied medical

Recall history

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

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