FDA Adverse Event
Injury
Summary report: N
TANDEM T: SLIM INSULIN DELIVERY SYSTEM
MDR report key: 3941026
·
Received June 30, 2014
Report
- Report Number
- 3007981285-2014-02026
- Event Type
- Injury
- Date Received
- June 30, 2014
- Date of Event
- May 14, 2014
- Report Date
- May 30, 2014
- Manufacturer
- TANDEM DIABETES CARE INC.
- Product Code
- LZG
- PMA / PMN Number
- K111210
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
THE DEVICE HAS NOT BEEN RETURNED FOR EVALUATION. SHOULD NEW INFORMATION BECOME AVAILABLE A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE CUSTOMER HAS EXPERIENCED HIGH BG LEVELS (200-350 MG/DL). THE CUSTOMER DOUBLED HIS DOSE OF INSULIN AND HIS BG LEVELS CAME DOWN. THE PUMP APPEARS TO BE FUNCTIONING AS INTENDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 378900 | TANDEM T: SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES CARE INC. | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 48 YR | Required Intervention |