FDAJune 9, 2017device

Sorin Group Aortic Arch Cannula, 7 mm x 10 in x 3/8 in, Rx Only, Sterile Product Usage: The Aortic Arch Cannulae are indicated for use in perfusion of the ascending aorta during cardiopulmonary bypass surgery.

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

The hazard

Identification of excess plastic on the tip of the cannula.

What to do

FDA enforcement status: Terminated

Brands named

sorin

Recall history

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

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