FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3965186 · Received July 29, 2014

Report

Report Number
1531186-2014-02857
Date Received
July 29, 2014
Date of Event
June 11, 2014
Report Date
June 18, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND

Narratives

Description of Event or Problem · 1

PER PROVIDER, CONSUMER STATES THAT ONE SIDE OF THE WALKER THE DUAL RELEASE PADDLE IS BROKEN THEREFORE IT WILL NO LONGER LOCK INTO PLACE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
440732 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 6291-3F

Patients

Seq Age Sex Outcome Treatment
1 Other