FDA Device recall Z-1355-2022
MiniMed 670G 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 670G 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-1355-2022 |
| 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 670G 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 (O.U.S. Version) MiniMed 670G (MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, MMT-1782, MMT-1760,…Product Number/CFN (O.U.S. Version) MiniMed 670G (MMT-1580, MMT-1581, MMT-1582, MMT-1780, MMT-1781, MMT-1782, MMT-1760, MMT-1761, MMT-1762, MMT-1883, MMT-1893) UDI-DI Codes: 643169946040 763000278427 763000179649 643169946057 763000096984 763000190453 763000283445 763000395858 763000367084 643169939202 763000166526 763000256821 763000283506 763000283513 763000365882 643169939219 763000090203 763000190460 763000283520 763000393786 Serial Numbers: U.S. NG1839499H NG1383785H NG2337855H NG2574462H NG2148562H NG1139337H NG2507207H NG1737004H NG1259251H NG2164126H NG2591910H NG1774415H NG2450722H NG2341546H NG2394493H NG1268923H NG2059875H NG1241089H NG2909394H NG2716073H NG1188783H NG1332358H NG1805098H NG1187471H NG1928485H NG2154209H NG2562452H NG1980564H NG1844854H NG1993223H NG2208062H NG1256182H NG2108291H NG2773622H NG2840625H NG2287463H NG2116702H NG2747513H NG2006685H NG2499718H NG2256617H NG1708020H NG2473735H NG2871000H NG2031708H NG3039842H NG2843313H NG2059984H NG2440836H NG177 |
|---|
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-1355-2022%22
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