Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MiniMed 770G Insulin Pump (U.S. and O.U.S. Version) Recalled by Medtronic MiniMed Due to Due to battery cap deterioration, this may potentially...
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 directly.
Affected Products
MiniMed 770G Insulin Pump (U.S. and O.U.S. Version)
Quantity: 123,585 pumps
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic MiniMed
Medtronic MiniMed has 31 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report