FDA Adverse Event Malfunction Summary report: N

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

MDR report key: 9416765 · Received December 5, 2019

Report

Report Number
3013756811-2019-89510
Event Type
Malfunction
Date Received
December 5, 2019
Date of Event
November 14, 2019
Report Date
December 5, 2019
Manufacturer
TANDEM DIABETES CARE
Product Code
OZO
UDI-DI
00853052007264
PMA / PMN Number
P180008
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT MULTIPLE TEMPERATURE ALARMS OCCURRED. CUSTOMER'S BLOOD GLUCOSE WAS BETWEEN 150-300 MG/DL. REPORTEDLY, THE CUSTOMER WILL CONTINUE TO USE THE PUMP FOR INSULIN THERAPY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1209866 T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY AUTOMATED INSULIN DOSING, THRESHOLD SUSPEND OZO TANDEM DIABETES CARE 1000096 00853052007264

Patients

Seq Age Sex Outcome Treatment
1 52 YR