FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3903286 · Received June 30, 2014

Report

Report Number
1531186-2014-02295
Date Received
June 30, 2014
Report Date
June 2, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

THE FROM WAS BROKEN ON THE LEFT HAND SIDE AT THE JOINT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
381097 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650

Patients

Seq Age Sex Outcome Treatment
1 Other