Penumbra’s Recall of the JET 7 Reperfusion Catheter

Penumbra is recalling the device due to distal tip damage

If your email program has trouble displaying this email, view as a webpage. Penumbra's Recall of the JET 7 Reperfusion Catheter Due to Distal Tip Damage Penumbra is recalling the JET7 Reperfusion Catheter because the catheter may become susceptible to distal tip damage during use.  Use of the affected product may cause serious injury or death. The FDA has identified this as a Class I recall, the most serious type of recall. Read the Recall Notice

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