Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1265-2025 — MiniMed insulin pump, REF: 770G (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)

U.S. FDA — Device Enforcement · United States · 2025-01-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1265-2025
Date of alert
2025-01-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic MiniMed, Inc.
Product category
device
Product type
Devices
Reported risk: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.