FDA Adverse Event Malfunction Summary report: N

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

MDR report key: 12789014 · Received November 10, 2021

Report

Report Number
3013756811-2021-125451
Event Type
Malfunction
Date Received
November 10, 2021
Date of Event
August 21, 2021
Report Date
November 10, 2021
Manufacturer
TANDEM DIABETES CARE
Product Code
QFG
UDI-DI
00853052007318
PMA / PMN Number
K201214
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, 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 THE CARTRIDGE WAS LEAKING FROM THE O-RING. CUSTOMER LOADED A NEW CARTRIDGE TO ADDRESS THE ISSUE. CUSTOMER'S BLOOD GLUCOSE WAS 110-160 MG/DL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1688091 T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG TANDEM DIABETES CARE 1000354 00853052007318

Patients

Seq Age Sex Outcome Treatment
1 40 YR Male INFUSION SET: AUTOSOFT 90INSULIN: NOVOLOG