FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2925970 · Received January 22, 2013

Report

Report Number
1531186-2013-00279
Date Received
January 22, 2013
Report Date
January 22, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PER DEALER THE BRAKE HOUSING IS BUSTED WHERE YOU TIGHTEN THE BRAKES. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
31457 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650

Patients

Seq Age Sex Outcome Treatment
1 Other