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Medtronic MiniMed recalls MiniMed 620G Insulin Pump (O.U.S. version)
Recalled July 20, 2022 · FDA recall Z-1352-2022 · Medtronic MiniMed
Hazard
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. · FDA Class II
Units
2,287 pumps
Sold at
U.S.: 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, and WY O.U.S.: Not provided
Description
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.
Product
MiniMed 620G Insulin Pump (O.U.S. version)
Manufacturer(s)
Medtronic MiniMed
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →