FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3200481 · Received July 1, 2013

Report

Report Number
1531186-2013-02893
Date Received
July 1, 2013
Report Date
June 7, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

PROVIDER STATES BROKEN AT THE CROSSBRACE WHERE IT OPENS UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
299267 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 6240-A

Patients

Seq Age Sex Outcome Treatment
1 Other