FDA Device recall Z-1771-2021
MiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6.5V BLE MMOL;¿ PUMP MMT-1886 MM780G 6.5W BLE MG
- FDA Device
- Class II
- ongoing
- Published 2021-06-09
On 2021-06-09 the FDA classified a Class II recall of MiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6.5V BLE MMOL;¿ PUMP MMT-1886 MM780G 6.5W BLE MG by Medtronic Minimed, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1771-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-03-15 |
| Published | 2021-06-09 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medtronic Minimed |
| Distribution | AR, CA, CO, CT, FL, GA, ID, MI, MN, TN, TX, WA |
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
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.
Identifiers
| code_info | Model#(CFN)/UDI-DI(GTIN): MMT-1885/00763000384258;¿ MMT-1886/00763000384265;¿ MMT-1895WW/00763000384272;¿ MMT-1896W…Model#(CFN)/UDI-DI(GTIN): MMT-1885/00763000384258;¿ MMT-1886/00763000384265;¿ MMT-1895WW/00763000384272;¿ MMT-1896WW/00763000384289;¿ MMT-1884XC/ 00763000455613;¿ MMT-1885XC/00763000421939;¿ MMT-1886XC/00763000421946;¿ MMT-1885L/00763000441432;¿ MMT-1886L/00763000441449;¿ MMT-1896ES/00763000454296;¿ MMT-1896WWA/00763000411541;¿ KIT MMT-1895WWA/00763000411374;¿ KIT MMT-1895WWA/00763000411381;¿ KIT MMT-1895WWA/00763000411398;¿ KIT MMT-1895WWA/00763000411404;¿ KIT MMT-1895WWA/00763000411411;¿ KIT MMT-1895WWA/00763000411428;¿ KIT MMT-1895WWA/00763000411435;¿ KIT MMT-1895WWA/00763000411459;¿ KIT MMT-1895WWA/00763000411466;¿ KIT MMT-1895WWA/00763000411473;¿ KIT MMT-1895WWA/00763000411497;¿ KIT MMT-1895WWA/00763000411503;¿ KIT MMT-1895WWA/00763000420703;¿ KIT MMT-1895WWA/00763000411510;¿ KIT MMT-1895WWA/00763000411527;¿ KIT MMT-1895WWA/00763000411534;¿ KIT MMT-1895WWA/00763000411565;¿ KIT MMT-1895WWA/00763000411572;¿ KIT MMT-1895WWA/00763000411596;¿ KIT MMT-1895 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1771-2021%22
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