FDA Adverse Event
Malfunction
Summary report: N
T:SLIM G5 SYSTEM
MDR report key: 7747863
·
Received August 3, 2018
Report
- Report Number
- 3013756811-2018-26028
- Event Type
- Malfunction
- Date Received
- August 3, 2018
- Date of Event
- July 13, 2018
- Report Date
- August 3, 2018
- Manufacturer
- TANDEM DIABETES CARE
- Product Code
- OYC
- UDI-DI
- 00853052007257519611
- PMA / PMN Number
- P140015
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- OTHER
Narratives
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 RECEIVED A POWER SOURCE ALERT LEADING TO THE PUMP BATTERY DEPLETING RAPIDLY AND SHUTTING DOWN. THE CUSTOMER'S BLOOD GLUCOSE LEVEL RANGED FROM 172-177 (MG/DL). REPORTEDLY, THE PUMP SUCCESSFULLY BEGAN CHARGING AFTER THE CUSTOMER PLUGGED THE PUMP BACK INTO THE POWER SOURCE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 587670 | T:SLIM G5 SYSTEM | CONTINUOUS GLUCOSE MONITOR | OYC | TANDEM DIABETES CARE | 1000096 | 00853052007257519611 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 49 YR |