FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 2990552 · Received March 5, 2013

Report

Report Number
1531186-2013-00874
Date Received
March 5, 2013
Date of Event
February 6, 2013
Report Date
February 6, 2013
Manufacturer
UNKNOWN
Product Code
ITJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

(B)(6) NOTICED THAT HIS REAR WHEEL IS BROKEN. HE WASN'T SURE HOW IT BECAME BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
94237 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN 66550

Patients

Seq Age Sex Outcome Treatment
1 Other