FDA Adverse Event Malfunction Summary report: N

SUNDASH

MDR report key: 2563080 · Received April 16, 2012

Report

Report Number
2311923-2012-00008
Event Type
Malfunction
Date Received
April 16, 2012
Date of Event
July 15, 2008
Report Date
April 16, 2012
Manufacturer
JK PRODUCTS & SERVICES, INC.
Product Code
LEJ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

COMPLAINANT CLAIMS TO HAVE REC'D AN INJURY FROM THE TANNING BED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SUNDASH 332 PRO1 LEJ JK PRODUCTS & SERVICES, INC. 332 PRO1 NA

Patients

Seq Age Sex Outcome Treatment
1 Other