FDA Adverse Event Injury Summary report: N

TWIIST AUTOMATED INSULIN DELIVERY SYSTEM

MDR report key: 24511770 · Received March 4, 2026

Report

Report Number
3016798778-2026-00047
Event Type
Injury
Date Received
March 4, 2026
Date of Event
February 2, 2026
Report Date
March 4, 2026
Manufacturer
MILLYARD ADVANCED MEDICAL PRODUCTS, LLC
Product Code
QFG
UDI-DI
00850017421400
PMA / PMN Number
K250930
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

BASED ON THE INFORMATION AVAILABLE FOR ASSESSMENT, A RELATIONSHIP BETWEEN THE TWIIST AUTOMATED INSULIN DELIVERY SYSTEM AND THE REPORTED SYMPTOMS COULD NOT BE DETERMINED. THE USER REMAINS ONGOING ON THEIR TWIIST PUMP. NO PRODUCT HAS BEEN RETURNED TO MILLYARD ADVANCED MEDICAL PRODUCTS, LLC FOR EVALUATION. INVESTIGATION INTO THE REPORTED EVENT REMAINS ONGOING. ANY RELEVANT INVESTIGATION RESULTS WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.

Description of Event or Problem · 0

AN INITIAL EVENT NOTIFICATION WAS RECEIVED BY MILLYARD ADVANCED MEDICAL PRODUCTS, LLC ON 02-FEB-2026. THE USER REPORTED THAT THEY EXPERIENCED A TOTAL OF TWO HYPOGLYCEMIC EVENTS ON (B)(6) 2026 AND THE WEEK OF (B)(6) 2026. THE USER REPORTED HAVING BLOOD GLUCOSE VALUES BETWEEN 34-37 MG/DL AND 54-55 MG/DL, RESPECTIVELY. THE USER REPORTED EXPERIENCING SYMPTOMS, INCLUDING SWEATING AND LETHARY, BUT CONFIRMED THEY DID NOT SEEK MEDICAL ATTENTION. THE USER RESOLVED THE EVENTS BY CONSUMING CARBOHYDRATES AND DRINKING JUICE. THE USER REMAINS ONGOING ON THE TWIIST AUTOMATED INSULIN DELIVERY SYSTEM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
402267 TWIIST AUTOMATED INSULIN DELIVERY SYSTEM INFUSION PUMP QFG MILLYARD ADVANCED MEDICAL PRODUCTS, LLC DKPI-21073-007 00850017421400

Patients

Seq Age Sex Outcome Treatment
1 38 YR Female Other