FDAJuly 24, 2015device

Medtronic EOPA Arterial Cannula, Model # 77620. Lot: 2015060544 intended to deliver oxygenated blood to the heart during cardiopulmonary bypass procedures for up to 6 hours in duration.

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

The hazard

EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.

What to do

FDA enforcement status: Terminated

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

Recall history

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

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Medtronic EOPA Arterial Cannula, Model # 77620. Lot: 2015060544 intended to deliver oxygenated blood to the heart during cardiopulmonary bypass procedures for up to 6 hours in duration. — Recall Details · AllClear