FDA Adverse Event Injury Summary report: N

ILET BIONIC PANCREAS

MDR report key: 23124216 · Received September 23, 2025

Report

Report Number
3019004087-2025-03371
Event Type
Injury
Date Received
September 23, 2025
Date of Event
August 26, 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 THE USER REPORTED HYPOGLYCEMIA WITH A LOWEST BLOOD GLUCOSE (BG) OF 65 MG/DL DURING A SUPPLY AND SENSOR CHANGE AFTER DROPPING AND BREAKING THE CARTRIDGE. THE USER TREATED WITH ORANGE JUICE, AND BG STABILIZED. NO MEDICAL INTERVENTION WAS REQUIRED, AND NO LONG-TERM HEALTH EFFECTS WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
219016 ILET BIONIC PANCREAS ALTERNATE CONTROLLER ENABLED INSULIN INFUSION PUMP QFG BETA BIONICS, INC. BB2001 33134

Patients

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