FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3181874 · Received June 21, 2013

Report

Report Number
1531186-2013-02736
Date Received
June 21, 2013
Date of Event
May 28, 2013
Report Date
May 28, 2013
Manufacturer
GENTEEL HOMECARE PRODUCTS
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER CLAIMS THAT THE ROLLATOR HAS A BENT FRAME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
282013 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ GENTEEL HOMECARE PRODUCTS 68100

Patients

Seq Age Sex Outcome Treatment
1 Other