FDA Adverse Event
Malfunction
Summary report: N
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
MDR report key: 4200232
·
Received October 22, 2014
Report
- Report Number
- 3007981285-2014-10408
- Event Type
- Malfunction
- Date Received
- October 22, 2014
- Date of Event
- September 27, 2014
- Report Date
- September 27, 2014
- Manufacturer
- TANDEM DIABETES CARE INC.
- Product Code
- LZG
- PMA / PMN Number
- K111210
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
THE PRODUCT HAS NOT BEEN RETURNED FOR EVAL. SHOULD NEW RELEVANT INFO BECOME AVAILABLE A SUPPLEMENTAL REPORT WILL BE SUBMITTED.
Description of Event or Problem · 1
THE CUSTOMER RECEIVED A MESSAGE DURING THE FILL TUBING PROCESS THAT THE CARTRIDGE NEEDED A MINIMUM OF 50 UNITS OF INSULIN TO PROCEED. REPORTEDLY, THE CARTRIDGE HAD BEEN FILLED WITH 180 UNITS OF COLD INSULIN. THERE WAS NO IMPACT TO THE CUSTOMER'S BLOOD GLUCOSE LEVEL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 673742 | TANDEM T:SLIM INSULIN DELIVERY SYSTEM | INSULIN PUMP | LZG | TANDEM DIABETES CARE INC. | 004628 | M004772 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 45 YR | INSULIN: HUMALOG| INFUSION SET: COMFORT SHORT |