Medtronic, Inc.
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
1 category · 2026-05-06 to 2026-05-06
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-05-06 | FDA Device | FDA Recall: Medtronic Sphere-9 Catheter, Model Number AFR-00001; catheter, percutaneous, cardiac ablation, for t | Medtronic, Inc. | Class II | N/A |