MiniMed 620G Insulin Pump — Class II medical device recall Z-1352-2022
Ongoing recall by Medtronic MiniMed, reported 2022-07-20, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to whe
| Recall number | Z-1352-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic MiniMed, Northridge, CA, United States |
| Recall initiated | 2022-05-23 |
| Classified | 2022-07-08 |
| Reported by FDA | 2022-07-20 |
| Distributed | 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, VI, VT, WA, WI, WV, WY |
| Quantity | 2,287 pumps |
| 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 and 475 more |
Product
MiniMed 620G Insulin Pump (O.U.S. version)
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1352-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.