Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic MiniMed Inc. Due to Medtronic is recalling the Medtronic MiniMed Paradigm Insulin...
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
Medtronic MiniMed Paradigm Insulin Infusion Pumps, Paradigm models: MMT-511, MMT-512, MMT-712, MMT-712E, MMT-515, MMT-715, MMT-522, MMT-522K, MMT-722, MMT-722K, MMT-523, MMT-523K, MMT-723, MMT-723K, MMT-554, and MMT-754. MiniMed 530G: MMT-551, and MMT-751 Paradigm insulin infusion pumps are intended for use to deliver basal and bolus insulin to persons with diabetes.
Quantity: 559,374 units total (444,374 units in US)
Why Was This Recalled?
Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps because they have received reports that users have accidentally programmed the pump to deliver the maximum bolus amount.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic MiniMed Inc.
Medtronic MiniMed Inc. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report