TWIIST AUTOMATED INSULIN DELIVERY SYSTEM
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
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.
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 |