Vascutek, Ltd.
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-03-11 to 2026-03-11
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-03-11 | FDA Device | FDA Recall: Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 6 | Vascutek, Ltd. | Class II | N/A |