Drug recall
Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072…
FDA recall event 99818 · Class II · Medtronic MiniMed, Inc.
Key facts
| Event ID | 99818 |
|---|---|
| Recall numbers | Z-0088-2027 |
| Recalling firm | Medtronic MiniMed, Inc. |
| Product type | Devices |
| Products | Brand Name: MiniMed Flex Product Name: MiniMed Flex Insulin Pump Model/Catalog Numbers: MMT-8062; MMT-8072 Product Description: The MiniMed Flex pump is an alternate controller enabled (ACE) pump… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Some MiniMed Flex insulin pumps were released with missing (i.e., devices with no result or abort test results are presumed to have failed) or failed verification test results in one or more of 9… |
| Initiation date | Aug 20, 2026 |
| Report date | Oct 14, 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: