Device recall
Z-0391-2022: Medical Device Identification Cards associated with Astra XT DR Implantable…
FDA device recall · Class II · Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Key facts
| Recall number (Z-number) | Z-0391-2022 |
|---|---|
| Recall event | 89054 |
| Product | Medical Device Identification Cards associated with Astra XT DR Implantable pulse generator |
| Product code | NVZ |
| Recalling firm | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 2026 |
| PMA numbers | P920015 |
| FEI number | 2182208 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
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