FDA Adverse Event
Malfunction
Summary report: N
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
MDR report key: 6354941
·
Received February 23, 2017
Report
- Report Number
- 3007981285-2017-05031
- Event Type
- Malfunction
- Date Received
- February 23, 2017
- Date of Event
- February 3, 2017
- Report Date
- February 23, 2017
- Manufacturer
- TANDEM DIABETES CARE
- Product Code
- LZG
- PMA / PMN Number
- K111210
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WV, US
- Reporter Occupation
- PATIENT
Narratives
Additional Manufacturer Narrative · 1
THE DEVICE IS EXPECTED TO BE RETURNED; HOWEVER, THE DEVICE HAS NOT YET BEEN RECEIVED. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF THE DEVICE IS RECEIVED. DEVICE NOT RETURNED.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE PUMP BATTERY DROPPED FROM 40% TO 5% SUDDENLY. FOLLOWING THE BATTERY DROP THE PUMP COULD NOT BE CHARGED DESPITE THE ATTEMPT OF MULTIPLE WALL ADAPTERS. CUSTOMER REPORTED BLOOD GLUCOSE LEVEL WAS 120-187 (MG/DL). REPORTEDLY THE CUSTOMER WILL CONTINUE TO USE THE PUMP FOR INSULIN THERAPY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 136455 | TANDEM T:SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES CARE | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 28 YR |