FDA Adverse Event Malfunction Summary report: N

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

MDR report key: 12224480 · Received July 26, 2021

Report

Report Number
3013756811-2021-79926
Event Type
Malfunction
Date Received
July 26, 2021
Date of Event
July 7, 2021
Report Date
July 26, 2021
Manufacturer
TANDEM DIABETES CARE
Product Code
QFG
UDI-DI
00850006613762
PMA / PMN Number
K201214
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

NO PRODUCT WAS RETURNED FOR EVALUATION. SHOULD NEW RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT A MALFUNCTION ALARM OCCURRED AND A CARTRIDGE CHANGE ERROR OCCURED. THE CUSTOMER RESET THE PUMP AND RELOADED A NEW CARTRIDGE TO RESOLVE THE ISSUES. CUSTOMER¿S BLOOD GLUCOSE LEVEL WAS 160-247 MG/DL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1122984 T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG TANDEM DIABETES CARE 1002717 M923567 00850006613762

Patients

Seq Age Sex Outcome Treatment
1 17 YR INSULIN: NOVOLOG/NOVORAPID