Device recall
Z-1533-2020: Medtronic Open Pivot Aortic Valve Graft, REF 502AG25, SIZE 25 mm
FDA device recall · Class II · MEDTRONIC ATS MEDICAL, INC.
Key facts
| Recall number (Z-number) | Z-1533-2020 |
|---|---|
| Recall event | 85092 |
| Product | Medtronic Open Pivot Aortic Valve Graft, REF 502AG25, SIZE 25 mm |
| Product code | LWQ |
| Recalling firm | MEDTRONIC ATS MEDICAL, INC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 4, 2022 |
| PMA numbers | P990046 |
| FEI number | 3008592544 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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