FDA Device recall Z-1359-2022
MiniMed 780G Insulin Pump (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 780G Insulin Pump (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-1359-2022 |
| 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 780G Insulin Pump (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 (O.U.S. Version) MiniMed 780G (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896) UDI Codes…Product Number/CFN (O.U.S. Version) MiniMed 780G (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896) UDI Codes: Pending Serial Numbers: U.S. (Clinical) NG2478545H NG2486895H NG2486985H NG2487001H NG2487055H NG2487108H NG2487112H NG2487154H NG2487171H NG2487193H NG2487198H NG2487262H NG2487277H NG2487329H NG2487331H NG2487334H NG2487385H NG2487392H NG2487395H NG2487400H NG2487403H NG2487405H NG2487409H NG2487410H NG2487419H NG2487426H NG2487430H NG2487431H NG2487451H NG2487461H NG2487479H NG2487488H NG2487490H NG2487491H NG2487500H NG2487503H NG2487506H NG2487507H NG2487570H NG2487577H NG2487583H NG2487590H NG2487639H NG2487660H NG2487675H NG2487688H NG2487701H NG2487703H NG2487710H NG2487731H NG2487732H NG2487769H NG2487775H NG2487776H NG2487784H NG2487790H NG2487793H NG2487833H NG2487836H NG2487844H NG2487847H NG2487860H NG2487862H NG2487865H NG2487887H NG2487892H NG2487964H NG2488018H NG2488067H NG2488106H NG2488163H NG2491860H NG2491901H NG2491927H NG2491932H NG2491935H NG2 |
|---|
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-1359-2022%22
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