FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4111294 · Received September 23, 2014

Report

Report Number
1531186-2014-04370
Date Received
September 23, 2014
Date of Event
August 27, 2014
Report Date
August 27, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER RECEIVED A CALL FROM CONSUMER WHO STATES THAT SOMETHING WAS WRONG WITH THE REAR LEG EXTENSIONS ON THIS WALKER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
589434 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 6291-5F

Patients

Seq Age Sex Outcome Treatment
1 Other