FDA Device recall Z-1356-2022
MiniMed 720G 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 720G 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-1356-2022 |
| 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 720G 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 720G (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1817, MMT-1867) UDI Codes…Product Number/CFN (O.U.S. Version) MiniMed 720G (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1817, MMT-1867) UDI Codes: Pending Serial Numbers (O.U.S.) NG2820120H NG2820133H NG2820138H NG2820180H NG2820183H NG2820193H NG2820227H NG2820238H NG2820239H NG2820241H NG2820242H NG2820253H NG2820256H NG2820258H NG2820282H NG2820295H NG2820339H NG2820341H NG2820357H NG2820366H NG2820368H NG2820371H NG2820372H NG2820374H NG2820377H NG2820379H NG2820381H NG2820386H NG2820387H NG2820388H NG2820393H NG2820394H NG2820396H NG2820398H NG2820400H NG2820401H NG2820409H NG2820418H NG2820421H NG2820425H NG2820428H NG2820432H NG2820435H NG2820437H NG2820457H NG2820460H NG2820462H NG2820463H NG2820467H NG2820472H NG2820484H NG2820487H NG2820489H NG2820494H NG2820496H NG2820498H NG2820501H NG2820503H NG2820510H NG2820512H NG2820513H NG2820518H NG2820522H NG2820523H NG2820525H NG2820529H NG2820533H NG2820535H NG2820539H NG2820542H NG2820549H NG2820557H NG2820559H NG2820561H NG2820567H NG2820569H NG2820571H |
|---|
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-1356-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.