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Medtronic MiniMed, Inc. Recall: Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754)

Medtronic MiniMed, Inc. Recall: Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754) is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Medtronic MiniMed, Inc.; Product: Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754); Reason for recall: All Medtronic MiniMed infusion pumps (Para

Recalling firmMedtronic MiniMed, Inc.
ProductParadigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754)
Reason for recallAll Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions rela
ClassificationClass II (moderate — may cause temporary or reversible health consequences)
StatusOngoing
DistributionWorldwide - US Nationwide distribution including in the states of OR, CA, AZ, NY,TX,FL, OH, MO, TN,NJ, NC, SC, IL, VA, WA, DC, GA, PA, MS,IA, MI, NH, OK, SD, MT, WI, WV, MA, LA, MN, RI, AR, ME, AL, IN, UT, KY, CO, ND, MD, CT, NM, KS, ID, NV, DE, NE, VT, AK, HI, WY, PR, VI and the countries of Taiwan
Recall initiated20260213
Recall numberZ-1752-2026
Categorydevice
StateCA
CountryUnited States

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