FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2973216 · Received February 21, 2013

Report

Report Number
1531186-2013-00692
Date Received
February 21, 2013
Report Date
February 21, 2013
Manufacturer
JUNCHENG
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4) - THE DEALER REPORTED THAT THE 6271 WALKER HAD A BROKEN WHEEL. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
75649 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ JUNCHENG 6271

Patients

Seq Age Sex Outcome Treatment
1 Other