FDA Adverse Event Malfunction Summary report: N

T:SLIM X2, BASAL-IQ, MMOL/L

MDR report key: 10006375 · Received April 28, 2020

Report

Report Number
3013756811-2020-40435
Event Type
Malfunction
Date Received
April 28, 2020
Date of Event
July 26, 2019
Report Date
April 28, 2020
Manufacturer
TANDEM DIABETES CARE
Product Code
OZO
PMA / PMN Number
P180008
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
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 RESISTANCE WAS EXPERIENCED DURING THE FILL PROCESS WITH MULTIPLE CARTRIDGES. CUSTOMER'S BLOOD GLUCOSE LEVEL RANGED BETWEEN 180-217 MG/DL. REPORTEDLY, SYRINGE NEEDLE CHANGES WERE PERFORMED TO ADDRESS THE ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
468406 T:SLIM X2, BASAL-IQ, MMOL/L AUTOMATED INSULIN DOSING, THRESHOLD SUSPEND OZO TANDEM DIABETES CARE 1002717 M368929

Patients

Seq Age Sex Outcome Treatment
1 33 YR