FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3140934 · Received June 3, 2013

Report

Report Number
1531186-2013-02390
Date Received
June 3, 2013
Report Date
May 3, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE DEALER IS REPORTING THAT THE DEVICE HAS BROKEN AT THE WELD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
244949 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65851B

Patients

Seq Age Sex Outcome Treatment
1 Other