FDA Adverse Event Malfunction Summary report: N

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

MDR report key: 15427567 · Received September 15, 2022

Report

Report Number
3013756811-2022-102279
Event Type
Malfunction
Date Received
September 15, 2022
Date of Event
August 21, 2022
Report Date
August 23, 2022
Manufacturer
TANDEM DIABETES CARE
Product Code
QFG
UDI-DI
00850006613793
PMA / PMN Number
K201214
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, 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 RESISTANCE WAS EXPERIENCED WHEN FILLING MULTIPLE CARTRIDGES WITH INSULIN. THE ISSUE WAS RESOLVED BY PERFORMING MULTIPLE CARTRIDGES CHANGES TO RESOLVE THE ISSUE CUSTOMER¿S BLOOD GLUCOSE WAS 250-270 MG/DL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
249557 T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG TANDEM DIABETES CARE 1000354 W0363149 00850006613793

Patients

Seq Age Sex Outcome Treatment
1 80 YR Female