FDA Adverse Event Malfunction Summary report: N

INSET II

MDR report key: 25122542 · Received May 8, 2026

Report

Report Number
3003442380-2026-15792
Event Type
Malfunction
Date Received
May 8, 2026
Date of Event
April 10, 2026
Report Date
April 13, 2026
Manufacturer
UNOMEDICAL DEVICES S.A DE C.V
Product Code
FPA
PMA / PMN Number
K032854
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

NAME: YPSOMED AG ADDRESS: WEISSENSTEINSTRASSE 26 CITY: SOLOTHURN COUNTRY: SWITZERLAND ZIP CODE: CH-4503. BASED ON THE AVAILABLE INFORMATION, THIS EVENT IS DEEMED TO BE A REPORTABLE MALFUNCTION. TO DATE NO ADDITIONAL INFORMATION HAS BEEN RECEIVED. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, A FOLLOW-UP REPORT WILL BE SUBMITTED. FDA REGISTRATION NUMBER REPORTING SITE: 8021545 MANUFACTURING SITE: 3003442380.

Description of Event or Problem · 0

IT WAS REPORTED THAT PATIENT FACED ISSUE WITH INFUSION SET ADHESIVE DOES NOT ADHERE EVENT ON 13 APR 2026.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
22842 INSET II Set, administration, intravascular FPA UNOMEDICAL DEVICES S.A DE C.V 86-060-52B6 6016082

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown