Penumbra recalls
Penumbra appears in 6 official U.S. recall notices indexed by RecallRadar, most recently on 2026-07-29.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
FDA Device · Class II · 2026-07-29 · Penumbra - Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtra Flex technology (JET 7 Xtra Flex) is a c…
FDA Device · Class I · 2021-01-27 · Penumbra - Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing REF 5MAXJET7L138KIT The Penumbra JET 7 Reperfusion Catheter with…
FDA Device · Class I · 2021-01-27 · Penumbra - Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Delivery Device + Hi-Flow Aspiration Tubing REF J7XKIT132 The Penumbra JET 7…
FDA Device · Class I · 2021-01-27 · Penumbra - Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing REF 5MAXJET7KIT The Penumbra JET 7 Reperfusion Catheter with Xtr…
FDA Device · Class I · 2021-01-27 · Penumbra - Penumbra 3D Revascularization Device It is indicated for used in the revascularization of patients with acute ischemic stroke secondary to…
FDA Device · Class I · 2017-07-26 · Penumbra