FDA Adverse Event
Malfunction
Summary report: N
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
MDR report key: 3922145
·
Received May 30, 2014
Report
- Report Number
- 3007981285-2014-00875
- Event Type
- Malfunction
- Date Received
- May 30, 2014
- Date of Event
- May 5, 2014
- Report Date
- May 5, 2014
- Manufacturer
- TANDEM DIABETES
- Product Code
- LZG
- PMA / PMN Number
- K111210
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UT, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
DURING FURTHER TROUBLESHOOTING IT WAS IDENTIFIED PT HAD SELF STARTED ON THE PUMP AND WAS NOT TRAINED. PT SINCE HAS BEEN TRAINED BY A TANDEM CLINICAL DIABETES SPECIALIST.
Description of Event or Problem · 1
RECEIVED INFO STATING PT WAS EXPERIENCING HIGH BG'S.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 319753 | TANDEM T:SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 29 YR |