FDA Reports Ongoing Recall of Medtronic Arterial Cannulas
An open Class II recall covers 1,424 arterial cannula units distributed worldwide due to potential pinhole leaks.
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An open Class II recall covers 1,424 arterial cannula units distributed worldwide due to potential pinhole leaks.
The agency has closed the recall of certain Medtronic arterial cannulas, considering it carried out.
The ongoing Class II recall covers 3,621 units of arterial return cannulas due to potential pinhole leaks.