Medtronic MiniMed, Inc.
Medtronic MiniMed, Inc.: 9 recalls listed since February 2026 across FDA.
By year
- 20269
By agency
- FDA9
By category
- Medical Device9
All recalls (9)
Medtronic MiniMed Go App
The MiniMed Go app has a software defect that can cause missed or delayed insulin doses, potentially leading to hyperglycemia or hypoglycemia.
Medtronic CareLink Clinic
CareLink Clinic software has a defect that can lead to incorrect insulin doses.
Medtronic MiniMed Flex Insulin Pumps
The MiniMed Flex insulin pump may have failed verification tests, leading to issues such as inaccurate insulin delivery.
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.
3 products
MiniMed Go App
The MiniMed Go App may miss nighttime alerts, leading to missed insulin doses and increased hyperglycemia risk.
MiniMed 780G Insulin Pump
The MiniMed 780G Insulin Pump can stop delivering insulin due to a software anomaly, leading to delayed therapy and increased risk of hyperglycemia or DKA.
Medtronic MiniMed and Paradigm Insulin Pumps
Over-delivery can cause severe hypoglycemia, altered mental status, seizure, coma, or death.
14 productsMedtronic MiniMed 780G Insulin Pumps
The MiniMed 780G insulin pump with software versions 6.60 and 6.61 has software defects that could cause hypoglycemia or hyperglycemia.
Medtronic MiniMed 780G Insulin Pump
A software issue may cause Pump Error 43 or 41, suspending insulin delivery.