FDAApril 1, 2022device

Flo-Thru Intraluminal Shunt. Used in coronary artery or peripheral vascular procedures. Used to shunt blood at the anastomosis to provide a temporary blood-free operative field for suturing while allowing blood to flow distal to the anastomosis.

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

The hazard

There is a potential for foreign matter.

What to do

FDA enforcement status: Completed

Brands named

baxter healthcarebaxter

Recall history

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

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