FDAJanuary 3, 2018device

Medtronic Custom Perfusion Systems, indicated for use in the extracorporeal circuit during cardiopulmonary bypass (CPB) surgical procedures.

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

The hazard

Medtronic custom perfusion tubing packs contain Terumo OPS valves that were recalled due to a lack of flow through the valve.

What to do

FDA enforcement status: Terminated

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

UPCs

208850741910380061399426817420643169876648006431698451210076300002587800643169845077006431698721270064316974159100643169735989006431699061812061399449076000643169471986

Recall history

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

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