Medtronic MiniMed Implantable Insulin Pump — Class II medical device recall Z-2173-2014
Terminated recall by Medtronic MiniMed Inc., reported 2014-08-20, distributed in NJ. Medtronic MiniMed is recalling the Implantable Insulin Pump because there have been reports of a pump malfunct
| Recall number | Z-2173-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic MiniMed Inc., Northridge, CA, United States |
| Recall initiated | 2014-06-16 |
| Classified | 2014-08-08 |
| Reported by FDA | 2014-08-20 |
| Terminated | 2014-09-25 |
| Distributed | NJ |
| Countries outside the US | BE, FR, SE |
| Quantity | 764 units |
| Reason classes | device malfunction |
| Model numbers | MMT-2007D |
Product
Medtronic MiniMed Implantable Insulin Pump, Model No. MMT-2007D
Reason for recall
Medtronic MiniMed is recalling the Implantable Insulin Pump because there have been reports of a pump malfunction resulting in the disconnection of the delivery of insulin prior to the end of the 7 year useful life of the device.
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-2173-2014. 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.