FDA Adverse Event Malfunction Summary report: N

MICROTOUCH PLUS GLOVES

MDR report key: 1630801 · Received March 10, 2010

Report

Report Number
MW5015102
Event Type
Malfunction
Date Received
March 10, 2010
Date of Event
March 9, 2010
Report Date
March 10, 2010
Manufacturer
ANSELL
Product Code
LYY
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

ICU STAFF REPORTED FAULTY GLOVES. THE GLOVES WERE WEAK AND WERE BREAKING EASILY WITH MULTIPLE HOLES. THIS WAS REPORTED TO THE PURCHASING DIRECTION FOR FOLLOW-UP. THE GLOVES WERE REMOVED FROM THE UNIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MICROTOUCH PLUS GLOVES LYY ANSELL 5004

Patients

Seq Age Sex Outcome Treatment
1 NA