FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3071866 · Received April 22, 2013

Report

Report Number
1531186-2013-01677
Date Received
April 22, 2013
Report Date
March 26, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. DEALER STATED THAT THE RIGHT SIDE BREAK PAD IS MISSING OFF THE BRAKE ASSEMBLY. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
171636 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 66550

Patients

Seq Age Sex Outcome Treatment
1 Other