MiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6 — Class II medical device recall Z-1771-2021
Ongoing recall by Medtronic Minimed, reported 2021-06-09, distributed in AR, CA, CO, CT, FL, GA, ID, MI…. Due to a software design issue, under certain conditions, a software fault is detected when a large bolus deli
| Recall number | Z-1771-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Minimed, Northridge, CA, United States |
| Recall initiated | 2021-03-15 |
| Classified | 2021-06-01 |
| Reported by FDA | 2021-06-09 |
| Distributed | AR, CA, CO, CT, FL, GA, ID, MI, MN, TN, TX, WA |
| Countries outside the US | AT, BE, BH, CH, CL, CZ, DE, DK, EG, ES, FI, FR, GB, GR, HR, HU, IE, IL, IS, IT, LU, MT, NL, NO, PL, QA, RO, SE, SI, TR, ZA |
| Quantity | 15,682 devices |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 00763000384258, 00763000384265, 00763000384272, 00763000384289, 00763000411374, 00763000411381, 00763000411398, 00763000411404, 00763000411411, 00763000411428, 00763000411435, 00763000411459, 00763000411466, 00763000411473, 00763000411497, 00763000411503, 00763000411510, 00763000411527, 00763000411534, 00763000411541, 00763000411558, 00763000411565, 00763000411572, 00763000411589, 00763000411596 and 9 more |
| Serial numbers | NG2, NG2357431H, NG2357433H, NG2357436H, NG2357444H, NG2357448H, NG2357449H, NG2357452H, NG2357455H, NG2357460H, NG2357463H, NG2357466H, NG2357468H, NG2357473H, NG2357483H, NG2357494H, NG2357495H, NG2357497H, NG2357505H, NG2357507H, NG2357520H, NG2357521H, NG2357526H, NG2357531H, NG2357533H and 475 more |
| Model numbers | 00763000455613, MMT-1884XC, MMT-1885/00763000384258, MMT-1885L/00763000441432, MMT-1885XC/00763000421939, MMT-1886/00763000384265, MMT-1886L/00763000441449, MMT-1886XC/00763000421946, MMT-1895WW/00763000384272, MMT-1895WWA/00763000411374, MMT-1895WWA/00763000411381, MMT-1895WWA/00763000411398, MMT-1895WWA/00763000411404, MMT-1895WWA/00763000411411, MMT-1895WWA/00763000411428, MMT-1895WWA/00763000411435, MMT-1895WWA/00763000411459, MMT-1895WWA/00763000411466, MMT-1895WWA/00763000411473, MMT-1895WWA/00763000411497, MMT-1895WWA/00763000411503, MMT-1895WWA/00763000411510, MMT-1895WWA/00763000411527, MMT-1895WWA/00763000411534, MMT-1895WWA/00763000411565 and 10 more |
Product
MiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6.5V BLE MMOL;¿ PUMP MMT-1886 MM780G 6.5W BLE MG; KIT MMT-1895WW MM780G 6.5V BLE SF MMOL;¿ KIT MMT-1896WW MM780G 6.5W BLE SF MG;¿ PUMP MMT-1884XC 780G V6.5 CLIN US MG;¿ PUMP MMT-1885XC 780G V6.5 CLIN MM;¿ PUMP MMT-1886XC 780G V6.5 CLIN MG;¿ PUMP MMT-1885L MM780G 6.5V BLE MMOL;¿ PUMP MMT-1886L MM780G 6.5W BLE MG;¿ KIT MMT-1896ES MM780G V6.5W MG;¿ KIT MMT-1896WWA MM780G BLE MG ES;¿ KIT MMT-1895WWA MM780G BLE MMOL AR;¿ KIT MMT-1895WWA MM780G BLE MMOL CS;¿ KIT MMT-1895WWA MM780G BLE MMOL DA;¿ KIT MMT-1895WWA MM780G BLE MMOL DE;¿ KIT MMT-1895WWA MM780G BLE MMOL EN;¿ KIT MMT-1895WWA MM780G BLE MMOL FI;¿ KIT MMT-1895WWA MM780G BLE MMOL FR;¿ KIT MMT-1895WWA MM780G BLE MMOL IT;¿ KIT MMT-1895WWA MM780G BLE MMOL NL;¿ KIT MMT-1895WWA MM780G BLE MMOL NO;¿ KIT MMT-1895WWA MM780G BLE MMOL SL; KIT MMT-1895WWA MM780G BLE MMOL SV;¿ KIT MMT-1895WWA MM780G BLE MMOL HU;¿ KIT MMT-1896WWA MM780G BLE MG AR;¿ KIT MMT-1896WWA MM780G BLE MG DE;¿ KIT MMT-1896WWA MM780G BLE MG EL;¿ KIT MMT-1896WWA MM780G BLE MG HE;¿ KIT MMT-1896WWA MM780G BLE MG IT;¿ KIT MMT-1896WWA MM780G BLE MG PL;¿ KIT MMT-1896WWA MM780G BLE MG RO;¿ KIT MMT-1896WWA MM780G BLE MG TR;¿ KIT MMT-1896WWA MM780G BLE MG NL;¿ KIT MMT-1896WWA MM780G BLE MG FR;¿ KIT MMT-1896WWA MM780G BLE MG ES;
Reason for recall
Due to a software design issue, under certain conditions, a software fault is detected when a large bolus delivery at quick bolus speed completes. if the user is not aware of the amount of active insulin and delivers an additional bolus, there is a risk of insulin over delivery.
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-1771-2021. 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.