FDA Adverse Event Injury Summary report: N

ILET BIONIC PANCREAS

MDR report key: 23129121 · Received September 23, 2025

Report

Report Number
3019004087-2025-03423
Event Type
Injury
Date Received
September 23, 2025
Date of Event
August 13, 2025
Report Date
September 23, 2025
Manufacturer
BETA BIONICS INC
Product Code
QFG
PMA / PMN Number
K231485
Adverse Event
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 (B)(6) 2025 IT WAS REPORTED THAT THE USER EXPERIENCED HYPOGLYCEMIA WITH BLOOD GLUCOSE (BG) LEVELS OF 30 MG/DL WHILE USING THE ILET. THE USER CORRECTED THE EVENT WITH JUICE AND DID NOT REQUIRE HOSPITALIZATION. NO LONG-TERM HEALTH EFFECTS WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
734221 ILET BIONIC PANCREAS ALTERNATE CONTROLLER ENABLED INFUSION PUMP QFG BETA BIONICS INC BB1001

Patients

Seq Age Sex Outcome Treatment
1 58 YR Female Other