FDA Adverse Event Malfunction Summary report: N

PREMIERPRO

MDR report key: 18490970 · Received January 11, 2024

Report

Report Number
18490970
Event Type
Malfunction
Date Received
January 11, 2024
Date of Event
October 17, 2023
Report Date
November 9, 2023
Manufacturer
SVS LLC
Product Code
FQM
Product Problem
Yes
Report Source
User Facility report
Reporter Location
AZ
Reporter Occupation
RISK MANAGER
Health Professional
N

Narratives

Description of Event or Problem · 0

PREMIERPRO ELASTIC BANDAGES EASILY TEAR AND BECOMES ABNORMALLY STICKY ONCE PATIENT FLUIDS TOUCH THE BANDAGE AND TRANSFERS ON TO OUR GLOVES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
954489 PREMIERPRO BANDAGE, ELASTIC FQM SVS LLC 8956 CDSM06-02

Patients

Seq Age Sex Outcome Treatment
1 25185 DA Unknown