FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3071879 · Received April 22, 2013

Report

Report Number
1531186-2013-01680
Date Received
April 22, 2013
Report Date
March 26, 2013
Manufacturer
UNKNOWN
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

PER DEALER BROKE AT CROSSBRACE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
172783 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650R

Patients

Seq Age Sex Outcome Treatment
1 Other