Medtronic Minimed, Inc.: Alternate Controller Enabled Insulin Infusion Pump
Recall Summary Medtronic MiniMed 780G insulin pumps (model numbers MMT-1885, MMT-1886, MMT-1895, MMT-1896) are being recalled due to a software problem that can cause the pump to unexpectedly stop delivering insulin when used with the Instinct sensor. When this happens, the pump displays two error messages in a row (Error 53 followed by Error 23), which interrupts insulin delivery and may delay treatment. This recall affects patients in Spain, Great Britain, the Netherlands, and Italy.
- Recalling firm
- Medtronic MiniMed, Inc.
- Product
- MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
- Reason
- A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and displays two error messages back-to-back: Pump Error 53 followed immediately by Pump Error 23. Insulin delivery will stop which may lead to delayed therapy and an increased risk of hyperglycemia or diabetic ketoacidosis (DKA).
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-05-27
- Status
- Open, Classified
- Distribution
- International distribution to the countries of Spain, Great Britain, Netherlands, Italy.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/74c45858-e77b-4138-93f0-178432873965