FDA Adverse Event Malfunction Summary report: N

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

MDR report key: 11467025 · Received March 11, 2021

Report

Report Number
3013756811-2021-25724
Event Type
Malfunction
Date Received
March 11, 2021
Date of Event
February 12, 2021
Report Date
March 11, 2021
Manufacturer
TANDEM DIABETES CARE
Product Code
OZO
PMA / PMN Number
K201214
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE NOT RETURNED.

Description of Event or Problem · 1

IT WAS REPORTED THAT AN OCCLUSION ALARM OCCURRED. CUSTOMER CHANGED THE PUMP SUPPLIES TO RESOLVE THE ISSUE. CUSTOMER'S BLOOD GLUCOSE WAS 180-270 MG/DL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
356016 T:SLIM X2, BASAL-IQ, MMOL/L AUTOMATED INSULIN DOSING, THRESHOLD SUSPEND OZO TANDEM DIABETES CARE 1002717

Patients

Seq Age Sex Outcome Treatment
1 63 YR