FDADecember 12, 2022device

Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF CB811. Used in Cardiopulmonary bypass.

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

The hazard

An upward trend of complaints in which the Temperature Monitoring Adapter (TMA), located on the Affinity Fusion Oxygenator, had come loose from the oxygenator either during pre-procedure perfusion set-up or post-procedure when disassembling the perfusion circuit.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

UPCs

006431695053220064316957226300643169618312006431696612950064316971340600643169724310006431697712600064316979218000643169930162006431699463920064316994976800643169976412

Recall history

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

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