FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2884505 · Received December 22, 2012

Report

Report Number
1531186-2012-01864
Date Received
December 22, 2012
Report Date
December 22, 2012
Manufacturer
GENTEEL HOMECARE PRODUCTS
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

(B)(4) - THE DEALER REPORTED THAT THE 6291-5F WALKER HAD A BENT FRAME BY THE HANDLE. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ GENTEEL HOMECARE PRODUCTS 6291-5F

Patients

Seq Age Sex Outcome Treatment
1 Other