FDA Device recall Z-1353-2022
MiniMed 630G Insulin Pump (U.S. and Canada Version)
- FDA Device
- Class II
- ongoing
- Published 2022-07-20
On 2022-07-20 the FDA classified a Class II recall of MiniMed 630G Insulin Pump (U.S. and Canada 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-1353-2022 |
| 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 630G Insulin Pump (U.S. and Canada 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 Canada Version) MiniMed 630G (MMT-1515, MMT-1714, MMT-1715, MMT-1755, MMT-1754) UDI-DI Co…Product Number/CFN (U.S. and Canada Version) MiniMed 630G (MMT-1515, MMT-1714, MMT-1715, MMT-1755, MMT-1754) UDI-DI Codes: 643169656840 763000090197 763000190439 763000316631 763000072520 763000166519 763000256807 763000316655 763000367053 643169752726 763000101527 763000157043 763000190446 763000317591 643169873841 643169878648 763000179632 763000317621 763000367091 Serial Numbers: U.S. NG1383785H NG2148562H NG1139337H NG1737004H NG1259251H NG1774415H NG1241089H NG1188783H NG1187471H NG1980564H NG1256182H NG2840625H NG2116702H NG2844148H NG2783673H NG1810845H NG2112005H NG2640743H NG2035194H NG2458619H NG2354215H NG2781208H NG2244550H NG1965419H NG2185247H NG2498398H NG1250806H NG1276438H NG2860063H NG2218677H NG2113185H NG2767104H NG2180341H NG1130892H NG2071932H NG2264667H NG1795581H NG2400221H NG2293843H NG2104120H NG2124365H NG2890094H NG2252300H NG1650442H NG1325260H NG1153291H NG2400741H NG2482730H NG2158681H NG1758986H NG2613364H NG1156096H NG1440806H NG2845051H NG1553883H NG |
|---|
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-1353-2022%22
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