Home » Penumbra Issues Recall for Reperfusion Catheters
Penumbra Issues Recall for Reperfusion Catheters
Penumbra is recalling one lot of its reperfusion catheters 032, which are used to re-establish blood supply to the brain in stroke victims. The recall comes as a result of a manufacturing error that causes mid-shaft joint failure in some of the catheters. The FDA has labeled the recall a Class I.
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