FDA Adverse Event Malfunction Summary report: N

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

MDR report key: 15658880 · Received October 24, 2022

Report

Report Number
3013756811-2022-117973
Event Type
Malfunction
Date Received
October 24, 2022
Date of Event
September 30, 2022
Report Date
October 24, 2022
Manufacturer
TANDEM DIABETES CARE
Product Code
QFG
UDI-DI
00389152000077
PMA / PMN Number
K201214
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

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

Description of Event or Problem · 0

IT WAS REPORTED THAT MULTIPLE CARTRIDGE ALARMS OCCURRED DURING BASAL DELIVERY. CUSTOMER'S BLOOD GLUCOSE LEVEL RANGED FROM 150-175 MG/DL. REPORTEDLY, THE CUSTOMER LOADED A NEW CARTRIDGE TO RESOLVE THE ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2591440 T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG TANDEM DIABETES CARE 1002717 00389152000077

Patients

Seq Age Sex Outcome Treatment
1 29 YR Male INSULIN: NOVOLOGINFUSION SET: VARISOFT