Device recall
Z-1238-2026: MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software…
FDA device recall · Class II · Medtronic MiniMed, Inc.
Key facts
| Recall number (Z-number) | Z-1238-2026 |
|---|---|
| Recall event | 97997 |
| Product | MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump is indicated for use by patients age 7-80 years with Type 1 diabetes, whose total daily dose of insulin is 8 units per day or more. The MiniMed 780G system is intended for continuous… |
| Product code | OZP |
| Recalling firm | Medtronic MiniMed, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K251032 |
| FEI number | 3003166194 |
At a glance
- 1–9 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