FDA Adverse Event Malfunction Summary report: N

ILET BIONIC PANCREAS

MDR report key: 23105397 · Received September 20, 2025

Report

Report Number
3019004087-2025-03218
Event Type
Malfunction
Date Received
September 20, 2025
Date of Event
August 24, 2025
Report Date
September 20, 2025
Manufacturer
BETA BIONICS INC
Product Code
QFG
PMA / PMN Number
K231485
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

AT THE TIME OF THIS REPORT THE ILET EVALUATION IS STILL IN PROGRESS. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN INVESTIGATION IS COMPLETED.

Description of Event or Problem · 0

ON 08/24/2025 THE PATIENT REPORTED TWO OCCLUSION ALARMS ON THE ILET BIONIC PANCREAS. DELIVERY WAS RESUMED AFTER EACH ALARM, AND BLOOD GLUCOSE WAS NOT AFFECTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2095068 ILET BIONIC PANCREAS ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG BETA BIONICS INC BB1001

Patients

Seq Age Sex Outcome Treatment
1 39 YR Female