FDA Adverse Event Malfunction Summary report: N

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

MDR report key: 13051665 · Received December 21, 2021

Report

Report Number
3013756811-2021-142662
Event Type
Malfunction
Date Received
December 21, 2021
Date of Event
December 11, 2021
Report Date
December 21, 2021
Manufacturer
TANDEM DIABETES CARE
Product Code
QFG
UDI-DI
00850006613762
PMA / PMN Number
K201214
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NM, 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 AN OCCLUSION OCCURRED. A SUPPLY CHANGE WAS PERFORMED RESOLVING THE OCCLUSION. CUSTOMER¿S BLOOD GLUCOSE LEVEL RANGED FROM 242-250 MG/DL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1952665 T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG TANDEM DIABETES CARE 1002717 00850006613762

Patients

Seq Age Sex Outcome Treatment
1 60 YR Female INSULIN: NOVOLOG