FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3103597 · Received May 9, 2013

Report

Report Number
1531186-2013-01993
Date Received
May 9, 2013
Report Date
April 15, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

ORDER NO. (B)(4)/LOT NUMBER 110315/BRAKE NOT RELEASING PER PROVIDER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
204408 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65851

Patients

Seq Age Sex Outcome Treatment
1 Other