FDAMay 7, 2018device

PROLENE SUTURE 4-36" (90CM) 3-0 BLUE, D6416

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

The hazard

The needle associated with certain suture product codes has the potential to perforate the packaging due to a packaging design issue. A perforated package has the potential to cause a soft tissue injury to a healthcare professional handling the subject product or a patient infection due to a breach of sterility within the packaging if it goes unnoticed by the healthcare professional.

What to do

FDA enforcement status: Terminated

Brands named

ethicon

Recall history

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

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