Data Foundry

Medical device recalls 2022

MiniMed 770G Insulin Pump — Class II medical device recall Z-1358-2022

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 numberZ-1358-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedtronic MiniMed, Northridge, CA, United States
Recall initiated2022-05-23
Classified2022-07-08
Reported by FDA2022-07-20
DistributedAK, 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
Quantity123,585 pumps
UPC / GTIN / UDI-DI00763000413750, 00763000414344, 00763000439859, 00763000439866
Serial numbersNG2, NG2438872H, NG2438899H, NG2438902H, NG2438905H, NG2439331H, NG2439816H, NG2439898H, NG2440061H, NG2440669H, NG2440698H, NG2440914H, NG2440958H, NG2441160H, NG2441169H, NG2441176H, NG2441453H, NG2441671H, NG2442203H, NG2442208H, NG2442308H, NG2442380H, NG2442741H, NG2442782H, NG2442880H and 475 more

Product

MiniMed 770G Insulin Pump (U.S. and 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-1358-2022. 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.