FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2884531 · Received December 22, 2012

Report

Report Number
1531186-2012-01857
Date Received
December 22, 2012
Report Date
December 21, 2012
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CT, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4) - THE DEALER REPORTED THAT THE 65350GR ROLLATOR HANDLE WAS BROKEN. THERE WAS NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65350GR

Patients

Seq Age Sex Outcome Treatment
1 Other