FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2851863 · Received November 29, 2012

Report

Report Number
1531186-2012-01540
Date Received
November 29, 2012
Report Date
November 29, 2012
Manufacturer
JUNCHENG
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE 6240-5F WALKER IS BROKEN AT A WELD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ JUNCHENG 6240-5F

Patients

Seq Age Sex Outcome Treatment
1 Other