FDA Adverse Event
Malfunction
Summary report: N
TANDEM T: SLIM INSULIN DELIVERY SYSTEM
MDR report key: 3905045
·
Received May 27, 2014
Report
- Report Number
- 3007981285-2014-00812
- Event Type
- Malfunction
- Date Received
- May 27, 2014
- Date of Event
- April 27, 2014
- Report Date
- April 27, 2014
- Manufacturer
- TANDEM DIABETES
- Product Code
- LZG
- PMA / PMN Number
- K111210
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
NO PRODUCT HAS BEEN RETURNED FOR EVALUATION. AS PER REPORTER IT IS NOT BELIEVED ALLEGED MALFUNCTION IS RELATED TO PUMP BUT TO A SITE ISSUE. IT IS UNKNOWN WHICH INFUSION SET WAS BEING USED AT THE TIME OF EVENT.
Description of Event or Problem · 1
RECEIVED INFORMATION STATING PATIENT WAS EXPERIENCING HIGH BG'S (300'S MG/DL).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 312008 | TANDEM T: SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 16 YR |