FDA Adverse Event Malfunction Summary report: N

T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 12146944 · Received July 9, 2021

Report

Report Number
3013756811-2021-74516
Event Type
Malfunction
Date Received
July 9, 2021
Date of Event
June 17, 2021
Report Date
July 9, 2021
Manufacturer
TANDEM DIABETES CARE
Product Code
LZG
UDI-DI
00852162004545
PMA / PMN Number
K111210
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PUMP INDICATED A DATA LOG CORRUPTION. ADDITIONALLY, THE PUMP TIME AND DATE WERE INCORRECT, CAUSE WAS UNKNOWN. THE CUSTOMER'S BLOOD GLUCOSE LEVEL WAS BETWEEN 163-249 MG/DL. DURING TROUBLESHOOTING WITH TANDEM TECHNICAL SUPPORT, THE CUSTOMER CORRECTED THE SETTINGS AND RESUMED INSULIN THERAPY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1040151 T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE 004628 00852162004545

Patients

Seq Age Sex Outcome Treatment
1 16 YR