MiniMed 670G Insulin Pump — Class II medical device recall Z-2981-2026
Ongoing recall by Medtronic MiniMed, Inc., reported 2026-08-26. Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump ca
| Recall number | Z-2981-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic MiniMed, Inc., Northridge, CA, United States |
| Recall initiated | 2026-07-13 |
| Classified | 2026-08-18 |
| Reported by FDA | 2026-08-26 |
| Countries outside the US | AT, BE, CH, DE, DK, GB, IE, IT, NL, SE |
| Quantity | 7 |
| UPC / GTIN / UDI-DI | 00763000404536, 00763000404543 |
| Serial numbers | NG2716176H, NG2748200H, NG2748664H, NG2755237H, NG3547582H |
| Model numbers | MMT-1781, MMT-1782 |
Product
MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Reason for recall
Loaner insulin pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2981-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.