FDA Adverse Event Malfunction Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3933939 · Received July 15, 2014

Report

Report Number
1525712-2014-03634
Event Type
Malfunction
Date Received
July 15, 2014
Report Date
June 6, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

PER DEALER THE GLIDE TIPS WEAR OUT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
412847 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 6291-A

Patients

Seq Age Sex Outcome Treatment
1 Other