FDA Adverse Event Malfunction Summary report: N

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 4240039 · Received October 29, 2014

Report

Report Number
3007981285-2014-11061
Event Type
Malfunction
Date Received
October 29, 2014
Date of Event
October 2, 2004
Report Date
October 2, 2014
Manufacturer
TANDEM DIABETES CARE INC.
Product Code
LZG
PMA / PMN Number
K111210
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

AN ADDITIONAL LOT NUMBER WAS REPORTED (LOT # M003484). HOWEVER, THE CAUSE OF THE EVENT IS NOT DUE TO THE CARTRIDGE.

Description of Event or Problem · 1

RECEIVED INFO REGARDING MULTIPLE CARTRIDGE ALARMS (CARTRIDGE ALARM 19) WITH MULTIPLE CARTRIDGES DURING THE LOAD PROCESS. REPORTEDLY, THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 200 MG/DL; HOWEVER, CUSTOMER STATED THAT ELEVATED BLOOD GLUCOSE LEVEL HAD NO RELATION TO CARTRIDGE ALARM 19.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
694235 TANDEM T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE INC. 004628 M001579

Patients

Seq Age Sex Outcome Treatment
1 14 YR