FDA Adverse Event Malfunction Summary report: N

TWIIST AUTOMATED INSULIN DELIVERY SYSTEM

MDR report key: 25262610 · Received May 22, 2026

Report

Report Number
3016798778-2026-00153
Event Type
Malfunction
Date Received
May 22, 2026
Date of Event
April 23, 2026
Report Date
May 22, 2026
Manufacturer
MILLYARD ADVANCED MEDICAL PRODUCTS, LLC
Product Code
QFG
UDI-DI
00850017421431
PMA / PMN Number
K250930
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NH, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION INTO THE REPORTED EVENT REMAINS ONGOING AND A SUPPLEMENTAL REPORT WILL BE FILED ONCE RESULTS ARE AVAILABLE. THE USER REMAINS ONGOING ON THEIR TWIIST PUMP. THE CURRENT VERSION OF THE TWIIST AUTOMATED INSULIN DELIVERY (AID) SYSTEM USER GUIDE PROVIDES INFORMATION ABOUT WAYS TO PREVENT HYPERGLYCEMIA. USERS ARE ALSO INSTRUCTED TO HAVE A BACKUP INSULIN THERAPY AVAILABLE AT ALL TIMES. NO ADDITIONAL INFORMATION RELEVANT TO THE REPORTED EVENT HAS BEEN MADE AVAILABLE TO MILLYARD ADVANCED MEDICAL PRODUCTS, LLC, AT THIS TIME.

Description of Event or Problem · 0

AN INITIAL EVENT NOTIFICATION WAS RECEIVED BY SEQUEL MED TECH, LLC, ON 23-APR-2026 AND FORWARDED TO MILLYARD ADVANCED MEDICAL PRODUCTS, LLC ON THE SAME DAY. THE USER REPORTED ELEVATED GLUCOSE LEVELS AND, WHILE ATTEMPTING A CORRECTION BOLUS, OBSERVED THAT THE PIGTAIL TUBING HAD DETACHED FROM THE BODY OF THE TWIIST CASSETTE. THE USER REPORTED THAT THEIR GLUCOSE INCREASED TO 303 MG/DL BEFORE REPLACING THE CASSETTE AND ADMINISTERING EXOGENOUS INSULIN. NO MEDICAL INTERVENTION WAS REQUIRED. THE USER REMAINS ONGOING ON THE TWIIST PUMP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
179302 TWIIST AUTOMATED INSULIN DELIVERY SYSTEM INFUSION PUMP QFG MILLYARD ADVANCED MEDICAL PRODUCTS, LLC DKPI-11073-001 00850017421431

Patients

Seq Age Sex Outcome Treatment
1