FDA recall, , Moderate risk
MiniMed 640G, 670G, and 780G Insulin Pump
Loaner insulin pumps may have been cleaned with chemically incompatible products, damaging the case or keypad and allowing moisture ingress.
Summary by Recall Canary from the FDA notice
What happened
Medtronic MiniMed, Inc., of Northridge, California, began a recall on July 13, 2026, for loaner MiniMed 670G, 780G, and 640G insulin pumps. The pumps may have been cleaned with chemically incompatible products that could damage the pump case or keypad, allow moisture ingress, and result in insulin over- or under-delivery, potentially causing hypoglycemia, hyperglycemia, or diabetic ketoacidosis.
The recall was added to the FDA's Enforcement Report and classified on August 18, 2026, with international distribution to Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, and Northern Ireland.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
3 products
Match the list below, then check the codes the FDA notice also names.
A UDI-DI is the device identifier printed with the barcode on the device label.
MiniMed 640G Insulin Pump
- Model
- MMT-1711
- UDI-DI
- 00763000404550
- 00763000404567
MiniMed 670G Insulin Pump
- Model
- MMT-1781
- UDI-DI
- 00763000404536
- 00763000404543
MiniMed 780G Insulin Pump
- Model
- MMT-1885CLW
- UDI-DI
- 00763000442187
- 00763000974374
- 00763000442194
- 00763000974381
From the FDA notice
MiniMed 640G Insulin Pump, Model: MMT-1711, MMT-1712;
Recall details
- Company began the recall
- Sold in
International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.
- Company
- Medtronic MiniMed, Inc.Northridge, California
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99374
- Recall numbers
- Z-2980-2026 to Z-2982-2026
All recalls from Medtronic MiniMed, Inc.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
