FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4091192 · Received September 16, 2014

Report

Report Number
1531186-2014-04134
Date Received
September 16, 2014
Report Date
August 22, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER: DAMAGED BRAKE ON LEFT REAR- CAUSING WHEEL TO RESTRICT MOVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
573745 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650

Patients

Seq Age Sex Outcome Treatment
1 Other