FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4213022 · Received October 30, 2014

Report

Report Number
1531186-2014-05213
Date Received
October 30, 2014
Report Date
October 9, 2014
Manufacturer
GENTEEL HOMECARE PRODUCTS
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER ALLEGES THE (B)(4) WALKER IS BENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
695736 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ GENTEEL HOMECARE PRODUCTS 6291-1

Patients

Seq Age Sex Outcome Treatment
1 Other