FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3100656 · Received May 8, 2013

Report

Report Number
1531186-2013-01951
Date Received
May 8, 2013
Report Date
April 11, 2013
Manufacturer
R. POON
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER THE BRAKE CABLE IS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
201601 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ R. POON 66500

Patients

Seq Age Sex Outcome Treatment
1 Other