FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4043559 · Received August 28, 2014

Report

Report Number
1531186-2014-03621
Date Received
August 28, 2014
Date of Event
July 25, 2014
Report Date
August 1, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER DEALER, ADVISED WHEEL IS CRACKED OUT OF BOX.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
525689 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650

Patients

Seq Age Sex Outcome Treatment
1 Other