FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3112755 · Received May 14, 2013

Report

Report Number
1531186-2013-02056
Date Received
May 14, 2013
Report Date
April 18, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

CONSUMER ALLEGES THAT THE FRAME BROKE ABOVE THE WELD RIGHT AT THE SEAT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
213215 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 65650

Patients

Seq Age Sex Outcome Treatment
1 Other