Drug recall
Medtronic, Simplera Sensor, REF: MMT-5100JD1
FDA recall event 96745 · Class II · Medtronic MiniMed, Inc.
Key facts
| Event ID | 96745 |
|---|---|
| Recall numbers | Z-0033-2026 |
| Recalling firm | Medtronic MiniMed, Inc. |
| Product type | Devices |
| Products | Medtronic, Simplera Sensor, REF: MMT-5100JD1 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The device cap label may not adhere to the sensor, compromising the sterility of the sensor, and increasing the risk of infection. |
| Initiation date | May 7, 2025 |
| Report date | Oct 8, 2025 |
| 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: