Recalls from Penumbra, Inc.

• Penumbra System (RED 62 Reperfusion Catheter) (opens in a new tab)
  Moderate risk, FDA, Sep 29, 2026, Manufacturing problem
• Penumbra System RED 68 Reperfusion Catheter (opens in a new tab)
  Moderate risk, FDA, Jul 21, 2026, Manufacturing problem

Data: Recall Canary (opens in a new tab)