Penumbra, Inc.
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-07-29 to 2026-07-29
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-07-29 | FDA Device | FDA Recall: Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT | Penumbra, Inc. | Class II | N/A |