FDA Adverse Event
Malfunction
Summary report: N
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
MDR report key: 3905214
·
Received May 29, 2014
Report
- Report Number
- 3007981285-2014-00863
- Event Type
- Malfunction
- Date Received
- May 29, 2014
- Date of Event
- April 30, 2014
- Report Date
- April 30, 2014
- Manufacturer
- TANDEM DIABETES CARE INC.
- Product Code
- LZG
- PMA / PMN Number
- K111210
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
CUSTOMER DID NOT WANT TO TROUBLESOOT HIGH BG'S AS SHE KNEW THAT SHE HAD FORGOTTEN TO BOLUS AND BELIEVED THAT WAS THE CAUSE.
Description of Event or Problem · 1
RECEIVED INFORMATION STATING PATIENT WAS EXPERIENCING HIGH BG'S (335 MG/DL) AS SHE HAD FORGOTTEN TO BOLUS EARLIER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 317393 | TANDEM T:SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES CARE INC. | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 19 YR |