Medtronic Minimed, Inc.: Alternate Controller Enabled Insulin Infusion Pump
Recall Summary Medtronic MiniMed is recalling certain loaner MiniMed 780G insulin pumps (models MMT-1885CLW and MMT-1886CLW) distributed in European countries because they may have been cleaned with incompatible chemicals that could damage the pump's case or keypad. This damage could allow moisture to enter the pump and cause it to deliver too much or too little insulin, potentially leading to dangerously high or low blood sugar levels or diabetic ketoacidosis. The recall affects loaner pumps in Germany, Denmark, Austria, the Netherlands, the United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, and Northern Ireland.
- Recalling firm
- Medtronic MiniMed, Inc.
- Product
- MiniMed 780G Insulin Pump, Model: MMT-1885CLW, MMT-1886CLW
- Reason
- Loaner insulin 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.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-07-13
- Status
- Open, Classified
- Distribution
- International distribution to the countries of Germany, Denmark, Austria, Netherlands, United Kingdom, Italy, Belgium, Ireland, Switzerland, Sweden, Northern Ireland.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a32c376d-6139-44c9-81f7-2b1c79eec879