Device recall
Z-2377-2018: Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554…
FDA device recall · Class II · Medtronic Inc.
Key facts
| Recall number (Z-number) | Z-2377-2018 |
|---|---|
| Recall event | 80320 |
| Product | Medtronic MiniMed Paradigm Veo Insulin Pump Product Catalog Number: MMT-554, MMT-754 |
| Product code | FPA |
| Recalling firm | Medtronic Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2022 |
| FEI number | 3003166194 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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