Drug recall
MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
FDA recall event 99207 · Class II · Medtronic MiniMed, Inc.
Key facts
| Event ID | 99207 |
|---|---|
| Recall numbers | Z-2698-2026 |
| Recalling firm | Medtronic MiniMed, Inc. |
| Product type | Devices |
| Products | MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back… |
| Initiation date | May 27, 2026 |
| Report date | Jul 15, 2026 |
| City | Northridge |
| State | CA |
| Country | United States |
| FEI number | 3003166194 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: