FDA Adverse Event Malfunction Summary report: N

T:SLIM INSULIN DELIVERY SYSTEM

MDR report key: 8160612 · Received December 13, 2018

Report

Report Number
3013756811-2018-46093
Event Type
Malfunction
Date Received
December 13, 2018
Date of Event
November 22, 2018
Report Date
December 13, 2018
Manufacturer
TANDEM DIABETES CARE
Product Code
LZG
UDI-DI
00852162004545
PMA / PMN Number
K111210
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, 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 THE CUSTOMER REMOVED THE PUMP CASE FROM THE PUMP AND THE CARTRIDGE WAS PULLED OUT. CUSTOMER'S BLOOD GLUCOSE RANGED BETWEEN 250-295 MG/DL. REPORTEDLY, THE CUSTOMER CONTINUED TO USE THE PUMP FOR INSULIN THERAPY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1001440 T:SLIM INSULIN DELIVERY SYSTEM INSULIN PUMP LZG TANDEM DIABETES CARE 004628 00852162004545

Patients

Seq Age Sex Outcome Treatment
1 68 YR