FDA Adverse Event
Malfunction
Summary report: N
TANDEM T: SLIM INSULIN DELIVERY SYSTEM
MDR report key: 3922138
·
Received May 30, 2014
Report
- Report Number
- 3007981285-2014-00873
- Event Type
- Malfunction
- Date Received
- May 30, 2014
- Date of Event
- May 5, 2014
- Report Date
- May 1, 2014
- Manufacturer
- TANDEM DIABETES
- 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
DURING FURTHER TROUBLESHOOTING IT WAS IDENTIFIED PATIENT IS USING APIDRA. CUSTOMER TECHNICAL SUPPORT HAS NOTIFIED REPORTER THAT APIDRA INSULIN IS CONTRAINDICATED FOR USE WITH T: SLIM.
Description of Event or Problem · 1
RECEIVED INFORMATION STATING PATIENT WAS EXPERIENCING HIGH BG'S (300 MG/DL).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 319822 | TANDEM T: SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES | 004628 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 32 YR |