FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3133623 · Received May 29, 2013

Report

Report Number
1531186-2013-02353
Date Received
May 29, 2013
Report Date
January 4, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

PROVIDER STATES BEARINGS CAME OUT OF REAR CASTER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
235937 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 66550

Patients

Seq Age Sex Outcome Treatment
1 Other