FDA Device recall Z-1352-2022
MiniMed 620G 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 620G 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-1352-2022 |
| 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 620G 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 620G (MMT-1510, MMT-1710, MMT-1750) UDI Code: Pending Serial Numbers: NG100…Product Number/CFN (O.U.S. version) MiniMed 620G (MMT-1510, MMT-1710, MMT-1750) UDI Code: Pending Serial Numbers: NG1003917H NG1004461H NG1010799H NG1012557H NG1020680H NG1026110H NG1028941H NG1028949H NG1028952H NG1028973H NG1034230H NG1034247H NG1034304H NG1034314H NG1034335H NG1034338H NG1034345H NG1034358H NG1034359H NG1034364H NG1034583H NG1034584H NG1034593H NG1034595H NG1034609H NG1035490H NG1035495H NG1035505H NG1035517H NG1035520H NG1035525H NG1035526H NG1035546H NG1035552H NG1035566H NG1035572H NG1035575H NG1035581H NG1035586H NG1035593H NG1035595H NG1035915H NG1035930H NG1035933H NG1035935H NG1036645H NG1036646H NG1036671H NG1036678H NG1036688H NG1036704H NG1036713H NG1036715H NG1036725H NG1036726H NG1036731H NG1036757H NG1036785H NG1036801H NG1036809H NG1036811H NG1036813H NG1036854H NG1039152H NG1040219H NG1040230H NG1040231H NG1040237H NG1040257H NG1040262H NG1040271H NG1040290H NG1040298H NG1040305H NG1040318H NG1040344H NG1040353H NG1040380H NG1040381H NG1040383H NG1040 |
|---|
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-1352-2022%22
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