FDADecember 12, 2024device

DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)

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

The hazard

Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

UPCs

2076300009110520763000091136

Recall history

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

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