INSPIREMD Inc
Frequent Recalls6
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-06-17 to 2026-06-17
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-06-17 | FDA Device | FDA Recall: Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840 | INSPIREMD Inc | Class II | N/A |
| 2026-06-17 | FDA Device | FDA Recall: Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830 | INSPIREMD Inc | Class II | N/A |
| 2026-06-17 | FDA Device | FDA Recall: CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030 | INSPIREMD Inc | Class II | N/A |
| 2026-06-17 | FDA Device | FDA Recall: CGuard Prime Carotid Stent System, 135cm, 9mx30mm Model/Catalog Number: CND0930 | INSPIREMD Inc | Class II | N/A |
| 2026-06-17 | FDA Device | FDA Recall: CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040 | INSPIREMD Inc | Class II | N/A |
| 2026-06-17 | FDA Device | FDA Recall: Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940 | INSPIREMD Inc | Class II | N/A |