FDA Adverse Event Malfunction Summary report: N

GUARDIAN ROLLING WALKER

MDR report key: 1032748 · Received April 18, 2008

Report

Report Number
3006459587-2008-00009
Event Type
Malfunction
Date Received
April 18, 2008
Date of Event
March 26, 2008
Report Date
April 9, 2008
Manufacturer
A&E
Product Code
ITJ
Product Problem
Yes
Report Source
Distributor report
Reporter Location
MI, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

THE THREADS OF THE LEG FOR THE FRONT CASTER WHEEL WERE STRIPPED. NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GUARDIAN ROLLING WALKER FOLDING WALKER ITJ A&E 07889T *

Patients

Seq Age Sex Outcome Treatment
1 *