FDA Adverse Event Malfunction Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 4120193 · Received September 25, 2014

Report

Report Number
1525712-2014-06338
Event Type
Malfunction
Date Received
September 25, 2014
Report Date
June 2, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER SEAT IS CRACKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
598219 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other