FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3140953 · Received June 3, 2013

Report

Report Number
1531186-2013-02389
Date Received
June 3, 2013
Report Date
May 3, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OK, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES THE WALKER LEG CRACKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
244386 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 6240-5F

Patients

Seq Age Sex Outcome Treatment
1 Other