FDA Adverse Event Summary report: N

MECHANICAL WALKER, ROLLATOR

MDR report key: 3747114 · Received April 11, 2014

Report

Report Number
1525712-2014-01874
Date Received
April 11, 2014
Date of Event
December 25, 2013
Report Date
March 14, 2014
Manufacturer
UNKNOWN
Product Code
ITJ
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

END USER ALLEGES DEFECTIVE ROLLATOR CAUSED SLIP/FALL ON SIDEWALK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
220549 MECHANICAL WALKER, ROLLATOR 890.3825 ITJ UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other