FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3915130 · Received July 7, 2014

Report

Report Number
1531186-2014-02407
Date Received
July 7, 2014
Date of Event
April 28, 2014
Report Date
June 3, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER, BROKEN AT CROSSBAR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
393450 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650

Patients

Seq Age Sex Outcome Treatment
1 Other