FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2760031 · Received September 26, 2012

Report

Report Number
1531186-2012-01024
Date Received
September 26, 2012
Report Date
September 25, 2012
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER CALLED STATING THAT THE RELEASE MECHANISM ON THE 6240-A ADULT WALKER HAS ALLEGEDLY SNAPPED OFF. NO INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 6240-A

Patients

Seq Age Sex Outcome Treatment
1 Other