Device recall
Z-0308-03: GEM DR Model 7271 Implantable Cardioverter-Defibrillator (ICD)
FDA device recall · Class II · Medtronic,Inc/Rice Creek Facil
Key facts
| Recall number (Z-number) | Z-0308-03 |
|---|---|
| Recall event | 25041 |
| Product | GEM DR Model 7271 Implantable Cardioverter-Defibrillator (ICD) |
| Recalling firm | Medtronic,Inc/Rice Creek Facil |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2182208 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database