FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2940322 · Received February 2, 2013

Report

Report Number
1531186-2013-00381
Date Received
February 2, 2013
Report Date
February 1, 2013
Manufacturer
GENTEEL HOMECARE PRODUCTS
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4) - THE DEALER REPORTED THAT THE 65100 ROLLATOR WELD CONNECTOR TO THE FRAME WAS BROKEN. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
45626 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ GENTEEL HOMECARE PRODUCTS 65100

Patients

Seq Age Sex Outcome Treatment
1 Other