Food, drugs, devices › Medtronic MiniMed Inc.
Device recall: Medtronic MiniMed Implantable Insulin Pump, Model No. MMT-2007D
FDA enforcement event 68633 is a device recall by Medtronic MiniMed Inc. of Northridge, CA, initiated 16 Jun 2014 and classified Class II, with 1 product record.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 91% of the 1,176 device enforcement events initiated in 2014 carry the same class.
Status: Terminated, terminated 25 Sep 2014. Initiation: voluntary: firm initiated. Medtronic MiniMed Inc. has 23 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Medtronic MiniMed Inc., Northridge, CA.
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."
Distribution
"New Jersey and Worldwide: Belgium, France, Netherland, and Sweden"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-2173-2014 | Medtronic MiniMed Implantable Insulin Pump, Model No. MMT-2007D | 764 units | Class II | Terminated | 20 Aug 2014 |
Context
Other enforcement events for Medtronic MiniMed Inc.
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 13 Jul 2026 | MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712; | Device | Class II | 3 |
| 16 Jun 2026 | MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android) | Device | Class II | 1 |
| 27 May 2026 | MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896 | Device | Class II | 1 |
| 13 Feb 2026 | MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782) | Device | Class II | 14 |
| 30 Jan 2026 | MiniMed" 780G - MMT-1884 MiniMed" 780G - MMT-1886 With Software 6.60 and 6.61 | Device | Class II | 1 |
| 13 Nov 2025 | InPen App, Model/CFN Number: MMT-8061 (Android Users) | Device | Class II | 1 |
| 2 Nov 2025 | MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump is | Device | Class II | 1 |
| 21 Oct 2025 | CareLink Clinic, REF: MMT-7350 | Device | Class II | 1 |
| 16 Jun 2025 | InPen App, CFN: MMT-8060 (iOS Users) and MMT-8061 (Android Users) | Device | Class II | 1 |
| 7 May 2025 | Medtronic, Simplera Sensor, REF: MMT-5100JD1 | Device | Class II | 1 |
All 23 events for Medtronic MiniMed Inc.
Questions and answers
Why was this device recalled?
FDA's record gives the reason for recall as: "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."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "New Jersey and Worldwide: Belgium, France, Netherland, and Sweden"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 25 Sep 2014. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.