FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3203310 · Received July 2, 2013

Report

Report Number
1531186-2013-02928
Date Received
July 2, 2013
Report Date
June 10, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

PER CONSUMER, THE SEAT IS BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
302944 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65350GR

Patients

Seq Age Sex Outcome Treatment
1 70 Other