Tandem Diabetes Care, Inc.
6495 Marindustry Place, San Diego, CA, US
Registered product codes
8 product codes
Recent MDR events
15,715 on file
- TANDEM MOBI INSULIN PUMPJul 16, 2026InjuryMW5190776
- TANDEM MOBI INSULIN PUMPJul 16, 2026InjuryMW5190777
- TANDEM MOBI INSULIN PUMPJul 16, 2026InjuryMW5190778
- TANDEM TSLIM X2Jul 8, 2026MalfunctionMW5190467
- TANDEM MOBIJul 1, 2026InjuryMW5190178
- TSLIM INSULIN PUMP X2Jun 17, 2026InjuryMW5189597
- TANDEM T:SLIM X2 AUTO SOFT 30 INSERTION SETJun 17, 2026InjuryMW5189612
- TANDEM MOBI INSULIN PUMPJun 10, 2026InjuryMW5189221
- TANDEM TSLIM X2 INSULIN PUMPJun 4, 2026MalfunctionMW5188926
- INSULIN PUMPJun 4, 2026InjuryMW5188949
Recalls
13 on file
- Open, ClassifiedMar 25, 2026
The Czech language user guide contained multiple translation errors. The most significant error was that it incorrectly instructs users to verify that the infusion set is connected to the body, when it should instead direct users to confirm that the infusion set is not connected to the body. Following this instruction could result in unintended insulin delivery, potentially leading to a hypoglycemic event.
View FDA record ↗ - Open, ClassifiedNov 5, 2025
Insulin pump includes a vibration motor that gives tactile feedback for any alerts, alarms, or malfunctions. Pump may exhibit false vibration motor failure due to a software issue causing Malfunction 12: "Pump cannot operate, the mobile app can no longer receive data from the pump. Insulin delivery and any active CGM Sessions have been stopped", which could result in hyperglycemia.
View FDA record ↗ - Open, ClassifiedOct 23, 2025
A software defect in versions 7.9.0.1 and 7.10.1 of the pump software for Tandem t:slim X2 and version 7.9.0.1 of the Tandem Mobi pump with Control-IQ+ technology that are paired with a G7 sensor may result in an unexpected automatic insulin correction bolus (autobolus ) which could result in hypoglycemia.
View FDA record ↗ - Open, ClassifiedSep 24, 2025
an app defect that occurs when the phone is set to a right-to-left language, which causes app-pump pairing issues and graphical defects, which can potentially lead to incorrect therapy decisions and subsequent hypoglycemia or hyperglycemia.
View FDA record ↗ - Open, ClassifiedAug 27, 2025
Insulin pumps manufactured with speakers from Revision A and B may malfunction ("Malfunction 16") which prevents audible alerts and causes the pumps to become inoperable and stop infusing insulin which could result in a hyperglycemic event, which may lead to injury and/or hospitalization.
View FDA record ↗ - Open, ClassifiedApr 11, 2025
A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is above 255 mg/dL at the start or end of a gap in data collection due to a lapse in connection from a paired continuous glucose monitor (CGM) sensor, which can lead to under-delivery or over-delivery of insulin based on inaccurate result leading to severe cases of hypoglycemia or hyperglycemia.
View FDA record ↗ - Open, ClassifiedApr 11, 2025
A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is above 255 mg/dL at the start or end of a gap in data collection due to a lapse in connection from a paired continuous glucose monitor (CGM) sensor, which can lead to under-delivery or over-delivery of insulin based on inaccurate result leading to severe cases of hypoglycemia or hyperglycemia.
View FDA record ↗ - Open, ClassifiedMay 6, 2024
During normal use, the mobile app version 2.7 may crash and be automatically relaunched by the iOS operating system. This cycle intermittently repeats, which leads to excessive Bluetooth communication that may result in pump battery drain and may lead to the pump shutting down sooner than typically expected. Pump shutdown will cause insulin delivery to suspend, which could lead to an under-delivery of insulin and may result in hyperglycemia, including severe hyperglycemia.
View FDA record ↗ - Open, ClassifiedSep 26, 2022
Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile Memory, 2) Inaccurate (Fluctuating) Battery Life Display, 3) Touchscreen Staying On, 4) Unexpected Open Loop, that can be mitigated with a software update. Issues could result in hypoglycemia, hyperglycemia or diabetic ketoacidosis.
View FDA record ↗ - Open, ClassifiedSep 26, 2022
Insulin pumps may have the following issues: 1) Malfunction 6 Non-Volatile Memory, 2) Inaccurate (Fluctuating) Battery Life Display, 3) Touchscreen Staying On, 4) Unexpected Open Loop, that can be mitigated with a software update. Issues could result in hypoglycemia, hyperglycemia or diabetic ketoacidosis.
View FDA record ↗
Compliance history
Matched by FEI 3016540876.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.