FDA Adverse Event Malfunction Summary report: N

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

MDR report key: 11353078 · Received February 19, 2021

Report

Report Number
3013756811-2021-20031
Event Type
Malfunction
Date Received
February 19, 2021
Date of Event
January 7, 2021
Report Date
February 19, 2021
Manufacturer
TANDEM DIABETES CARE
Product Code
OZO
UDI-DI
00850006613700
PMA / PMN Number
K201214
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NM, 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'S PUMP CASE WOULD NOT CLIP SECURELY. SUBSEQUENTLY, THE PUMP CASE FELL, CAUSING INFUSION SETS TO BE PULLED OUT. CUSTOMER'S BLOOD GLUCOSE WAS 202-224 MG/DL. THE CUSTOMER CHANGED INFUSION SET AND RESUMED INSULIN DELIVERY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
250003 T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY AUTOMATED INSULIN DOSING, THRESHOLD SUSPEND OZO TANDEM DIABETES CARE 1002717 00850006613700

Patients

Seq Age Sex Outcome Treatment
1 69 YR