Device recall
Z-1890-2017: MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below…
FDA device recall · Class II · Medtronic Inc.
Key facts
| Recall number (Z-number) | Z-1890-2017 |
|---|---|
| Recall event | 76436 |
| Product | MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected. Catalog Numbers for these insulin pumps are MMT-1510, MMT-1710, MMT-1711, MMT-1712. |
| Recalling firm | Medtronic Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 2017 |
| FEI number | 3003166194 |
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