FDA Device recall Z-1358-2022
MiniMed 770G Insulin Pump (U.S. and O.U.S. Version)
- FDA Device
- Class II
- ongoing
- Published 2022-07-20
On 2022-07-20 the FDA classified a Class II recall of MiniMed 770G Insulin Pump (U.S. and O.U.S. Version) by Medtronic Minimed, citing due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of t….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1358-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-05-23 |
| Published | 2022-07-20 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medtronic Minimed |
| Distribution | AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
Product
MiniMed 770G Insulin Pump (U.S. and O.U.S. Version)
Reason
Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps.
Identifiers
| code_info | Product Number/CFN (U.S. and O.U.S. Version) MiniMed" 770G pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-…Product Number/CFN (U.S. and O.U.S. Version) MiniMed" 770G pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892) UDI-DI Codes: 763000413750 763000439866 763000414344 763000439859 Serial Numbers: U.S. NG2574462H NG2507207H NG2591910H NG2450722H NG2909394H NG2562452H NG2773622H NG2747513H NG2499718H NG2871000H NG3039842H NG2962106H NG2522230H NG2752787H NG2613810H NG2583058H NG2491224H NG2581838H NG2603110H NG2463710H NG2497307H NG2514402H NG2713369H NG2823275H NG2495711H NG2456706H NG2546535H NG2811181H NG2642457H NG2542689H NG2878631H NG2533834H NG2614812H NG2656169H NG2530373H NG2614196H NG2656857H NG2488084H NG2644432H NG2641394H NG2922162H NG2583381H NG2982740H NG2659486H NG2635500H NG2773665H NG2750822H NG2569688H NG2719815H NG2509897H NG2593191H NG2613613H NG2509074H NG2642600H NG2498351H NG2467403H NG2614448H NG2446285H NG2787601H NG3040387H NG2534927H NG2968936H NG2912599H NG2616916H NG2512410H NG2672631H NG2562612H NG2542395H NG2752089H NG2869829H NG2495443H NG2918 |
|---|
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-1358-2022%22
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