FDA Adverse Event Other Summary report: N

TOWELS OR GREEN

MDR report key: 981904 · Received January 14, 2008

Report

Report Number
MW5005018
Event Type
Other
Date Received
January 14, 2008
Date of Event
January 10, 2008
Report Date
January 14, 2008
Manufacturer
A PLUS INTERNATIONAL
Product Code
KKX
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
KS, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

GREEN TOWELS FROM SET UP PACK APPEARED TO HAVE LEECHED GREEN ONTO THE SCRUB NURSES GLOVES. DATES OF USE: 2008. DIAGNOSIS OR REASON FOR USE: OPEN HEART SURGERY - IN SURGERY SET UP PACK. SINGLE USE DEVICE BUT KHH DISCARDS AFTER EACH PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOWELS OR GREEN SURGICAL TOWEL KKX A PLUS INTERNATIONAL 726269 - PACK

Patients

Seq Age Sex Outcome Treatment
1 70 YR Other