FDA Adverse Event Malfunction Summary report: N

ILET BIONIC PANCREAS

MDR report key: 23115063 · Received September 22, 2025

Report

Report Number
3019004087-2025-03292
Event Type
Malfunction
Date Received
September 22, 2025
Date of Event
July 28, 2025
Report Date
September 22, 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 25-AUG-2025, THE USER REPORTED THAT THE ILET WOULD NOT CHARGE OR REMAIN POWERED ON, CYCLING ON AND OFF DESPITE MULTIPLE CHARGERS BEING USED. A REPLACEMENT PUMP WAS ISSUED. NO SYMPTOMS WERE REPORTED, AND NO MEDICAL INTERVENTION WAS REQUIRED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2527153 ILET BIONIC PANCREAS ALTERNATE CONTROLLER ENABLED INSULIN INFUSION PUMP QFG BETA BIONICS, INC. BB1001

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown DEXCOM G7 CONTINUOUS GLUCOSE MONITOR