FDA Adverse Event
Malfunction
Summary report: N
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
MDR report key: 4240039
·
Received October 29, 2014
Report
- Report Number
- 3007981285-2014-11061
- Event Type
- Malfunction
- Date Received
- October 29, 2014
- Date of Event
- October 2, 2004
- Report Date
- October 2, 2014
- Manufacturer
- TANDEM DIABETES CARE INC.
- Product Code
- LZG
- PMA / PMN Number
- K111210
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
AN ADDITIONAL LOT NUMBER WAS REPORTED (LOT # M003484). HOWEVER, THE CAUSE OF THE EVENT IS NOT DUE TO THE CARTRIDGE.
Description of Event or Problem · 1
RECEIVED INFO REGARDING MULTIPLE CARTRIDGE ALARMS (CARTRIDGE ALARM 19) WITH MULTIPLE CARTRIDGES DURING THE LOAD PROCESS. REPORTEDLY, THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 200 MG/DL; HOWEVER, CUSTOMER STATED THAT ELEVATED BLOOD GLUCOSE LEVEL HAD NO RELATION TO CARTRIDGE ALARM 19.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 694235 | TANDEM T:SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES CARE INC. | 004628 | M001579 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 14 YR |