FDA Adverse Event Malfunction Summary report: N

UNO INSET II 60/6 BLUE TCAP 10PK INT

MDR report key: 19678362 · Received July 5, 2024

Report

Report Number
3003442380-2024-12286
Event Type
Malfunction
Date Received
July 5, 2024
Date of Event
May 24, 2024
Report Date
July 5, 2024
Manufacturer
UNOMEDICAL A/S
Product Code
FPA
UDI-DI
05705244018303
PMA / PMN Number
K032854
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

INITIAL AND FINAL MDR 1903609- MDR 3003442380-2024-12286- DEVICE 1 OF 5

Description of Event or Problem · 0

UNOMEDICAL REFERENCE NUMBER (B)(4). EVENT OCCURRED IN THE (B)(6) IT WAS REPORTED THAT INFUSION SET FELL OFF DURING USE. CALLER REPLACED INFUSION SET AND RESUMED INSULIN SUCCESSFULLY. NO FURTHER INFORMATION AVAILABLE

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1133799 UNO INSET II 60/6 BLUE TCAP 10PK INT AUTOSOFT 90 FPA UNOMEDICAL A/S 1002823 UNKNOWN 05705244018303

Patients

Seq Age Sex Outcome Treatment
1 NA Prefer Not To Disclose