FDA Adverse Event
Malfunction
Summary report: N
T:SLIM X2, BASAL-IQ, MMOL/L
MDR report key: 10483045
·
Received September 2, 2020
Report
- Report Number
- 3013756811-2020-97145
- Event Type
- Malfunction
- Date Received
- September 2, 2020
- Date of Event
- August 13, 2020
- Report Date
- September 2, 2020
- Manufacturer
- TANDEM DIABETES CARE
- Product Code
- OZO
- UDI-DI
- 00850006613021
- PMA / PMN Number
- P180008
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 0
IT WAS REPORTED THAT THE CUSTOMER EXPERIENCED AN UNEXPECTED RESET ALARM. CUSTOMER'S BLOOD GLUCOSE WAS 131-132 MG/DL. THE CUSTOMER WAS ABLE TO LOAD A NEW CARTRIDGE AND RESUME INSULIN DELIVERY.
Additional Manufacturer Narrative · 1
NO PRODUCT WAS RETURNED FOR EVALUATION. SHOULD NEW RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE CUSTOMER'S PUMP SHUTDOWN UNEXPECTEDLY. CUSTOMER'S BLOOD GLUCOSE WAS 131-132 MG/DL. THE CUSTOMER WAS ABLE TO LOAD A NEW CARTRIDGE AND RESUME INSULIN DELIVERY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 946269 | T:SLIM X2, BASAL-IQ, MMOL/L | AUTOMATED INSULIN DOSING, THRESHOLD SUSPEND | OZO | TANDEM DIABETES CARE | 1002717 | 00850006613021 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 18 YR |