Device recall
Z-0003-2025: MiniMed Insulin Pump Device. MiniMed 670G, REF: MMT-1580, MMT-1581, MMT-1582…
FDA device recall · Class I · Medtronic MiniMed, Inc.
Key facts
| Recall number (Z-number) | Z-0003-2025 |
|---|---|
| Recall event | 95121 |
| Product | MiniMed Insulin Pump Device. MiniMed 670G, REF: MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, MMT-1782, MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762; MiniMed 770G, REF: MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892; MiniMed 780G, REF: MMT-1884, MMT-1885, MMT-1886… |
| Product code | OZP |
| Recalling firm | Medtronic MiniMed, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| PMA numbers | P160017 |
| FEI number | 3003166194 |
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