FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3022128 · Received March 26, 2013

Report

Report Number
1531186-2013-01284
Date Received
March 26, 2013
Report Date
February 27, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

(B)(4) THE DEALER REPORTED THAT THE (B)(4) ROLLATOR BRAKE ASSEMBLY SPRING WAS BROKEN. THERE WAS NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
123305 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65851R

Patients

Seq Age Sex Outcome Treatment
1 Other