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FDANovember 4, 2015device

Thin-Flex Venous Cannula, Model Number:TF292902A

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

The hazard

Edwards Lifesciences initiated a field action for the Thin-Flex Venous Cannula (Model TF292902A) because the connector size is incorrectly described in the Edwards product guide as 3/8 inch. The actual and correct connector size is 1/2 inch.

What to do

FDA enforcement status: Terminated

Brands named

edwards lifesciencesedwards

Recall history

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

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