Device recall
Z-0561-2021: Evolut (TM) PRO+ System. With the following model numbers: a. EVPROPLUS-23US…
FDA device recall · Class II · Medtronic Heart Valves Division
Key facts
| Recall number (Z-number) | Z-0561-2021 |
|---|---|
| Recall event | 86681 |
| Product | Evolut (TM) PRO+ System. With the following model numbers: a. EVPROPLUS-23US, Labeled as VLV EVPROPLUS-23US COMM JPN, VLV EVPROPLUS-23 COMM US; b. EVPROPLUS-26US, Labeled as VLV EVPROPLUS-26US COMM JPN, VLV EVPROPLUS-26 COMM US; c. EVPROPLUS-29US, Labeled as VLV EVPROPLUS-29US COMM JPN, VLV… |
| Product code | NPT |
| Recalling firm | Medtronic Heart Valves Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 22, 2022 |
| PMA numbers | P130021 |
| FEI number | 2025587 |
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