FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3163556 · Received June 11, 2013

Report

Report Number
1531186-2013-02539
Date Received
June 11, 2013
Report Date
May 15, 2013
Manufacturer
HEALTHPLUS
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES THE BLUE RELEASE MECHANISM IS NOT WORKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
264503 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ HEALTHPLUS 6240-A

Patients

Seq Age Sex Outcome Treatment
1 Other