Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic MiniMed, Inc. directly.
Affected Products
MiniMed insulin pump, REF: 770G (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
Quantity: 106,289 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic MiniMed, Inc.
Medtronic MiniMed, Inc. has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report