FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2932083 · Received January 28, 2013

Report

Report Number
1531186-2013-00335
Date Received
January 28, 2013
Report Date
January 28, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES LEFT SIDE WILL NOT LOCK INTO PLACE. NO INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
38223 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other