Medtronic MiniMed Paradigm Insulin Infusion Pumps — Class II medical device recall Z-2544-2014
Terminated recall by Medtronic MiniMed Inc., reported 2014-09-03, distributed nationwide. Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps because they have received report
| Recall number | Z-2544-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic MiniMed Inc., Northridge, CA, United States |
| Recall initiated | 2014-03-13 |
| Classified | 2014-08-22 |
| Reported by FDA | 2014-09-03 |
| Terminated | 2015-04-07 |
| Distributed | Nationwide (US) |
| Model numbers | MMT-511, MMT-512, MMT-515, MMT-522, MMT-522K, MMT-523, MMT-523K, MMT-554, MMT-712, MMT-712E, MMT-715, MMT-722, MMT-722K, MMT-723, MMT-723K, MMT-754 |
Product
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.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2544-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.