FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2853629 · Received December 3, 2012

Report

Report Number
1531186-2012-01533
Date Received
December 3, 2012
Report Date
November 29, 2012
Manufacturer
GEOBY PEREGON HEALTHCARE PRODUCTS CO., LTD
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

ON (B)(6), THE DEALER REPORTED THAT THE 6100 ROLLATOR BRAKE CABLE WAS BROKEN. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ GEOBY PEREGON HEALTHCARE PRODUCTS CO., LTD 67100

Patients

Seq Age Sex Outcome Treatment
1 Other