FDA Adverse Event Malfunction Summary report: N

ERGOLINE

MDR report key: 2546892 · Received April 16, 2012

Report

Report Number
9615023-2012-00004
Event Type
Malfunction
Date Received
April 16, 2012
Date of Event
September 12, 2009
Report Date
April 16, 2012
Manufacturer
JK PRODUCTS GMBH
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

CLAIMANT ALLEGES TANNING BED CAUSED FIRE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ERGOLINE CLASSIC 600 LEJ JK PRODUCTS GMBH CLASSIC 600 NA

Patients

Seq Age Sex Outcome Treatment
1 Other