We pull official government recall records and translate each one into plain language: what happened, how serious it is, and the steps to take. No legalese.
Search by meaning, not just keywords — describe the product or the hazard and we’ll find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Medtronic Perfusion Systems recalls EOPA Elongated One-Piece Arterial Cannula DIL TIP 22FR due to pinhole leaks during cardiopulmonary bypass that may cause hypovolemia, vessel laceration, or organ dysfunction. Affected units have specific model and lot numbers.
Medtronic recalls EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR for possible pinhole leaks during cardiopulmonary bypass that could cause bleeding, vessel damage, or organ failure.
Medtronic Perfusion Systems recalls EOPA 3D Arterial Cannula DIL TIP 22FR used in cardiopulmonary bypass. Pinhole leaks may cause hypovolemia, vessel laceration, or organ dysfunction. Affected units have specific model and lot numbers.
Medtronic Perfusion Systems recalls EOPA 3D Arterial Cannula 22FR model 78322 due to potential pinhole leaks during cardiopulmonary bypass that could cause hypovolemia, vessel laceration, or organ dysfunction.
