FDAMay 17, 2019device

SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA, SIG45AXT

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

The hazard

The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.

What to do

FDA enforcement status: Ongoing

Brands named

covidien

Recall history

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

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