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Medtronic Inc. recalls Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965
Recalled November 29, 2017 · FDA recall Z-0110-2018 · Medtronic
Hazard
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin. · FDA Class II
Units
1,513,530 units
Sold at
Worldwide
Description
Medtronic MiniMed(TM) Infusion Sets have the potential for over-delivery of Insulin.
Product
Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T)
Manufacturer(s)
Medtronic Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →