FDA Adverse Event Summary report: N

EQUASHIELD

MDR report key: 1920569 · Received November 17, 2010

Report

Report Number
1920569
Date Received
November 17, 2010
Date of Event
October 27, 2010
Report Date
November 17, 2010
Manufacturer
EQUASHIELD
Product Code
FPA
Report Source
User Facility report
Reporter Location
OH, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

WHILE GIVING IV PUSH CHEMOTHERAPY THROUGH THE DEVICE, THERE WAS A FLUID LEAK.====================== HEALTH PROFESSIONAL'S IMPRESSION======================CHEMO LEAKED THROUGH THE DEVICE AND ONTO THE BED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EQUASHIELD EQUASHIELD FPA EQUASHIELD REF:LL-1 10-2110

Patients

Seq Age Sex Outcome Treatment
1 27 YR CHEMOTHERAPY