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U.S. Department of Health and Human Services

Class 2 Device Recall NANNOLIGHT INTENSE PULSED LIGHT SYSTEM

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  Class 2 Device Recall NANNOLIGHT INTENSE PULSED LIGHT SYSTEM see related information
Date Initiated by Firm April 12, 2008
Date Posted September 03, 2009
Recall Status1 Terminated 3 on July 05, 2012
Recall Number Z-1444-2009
Recall Event ID 51704
510(K)Number K082033  
Product Classification Powered laser surgical instrument - Product Code GEX
Product Sybaritic, NannoLight MP50.


Model Numbers and Description:
1.) 304207-MP 220 Volt, Multi-Platform configuration (able to attach optional
laser handpiece when purchased separately), Subassembly
(unit only, no safety glasses, owner's manual, etc. included);

2.) 404207 Completed unit (safety glasses, owner's manual, etc. included), glossy finish, 220 Volt;


3.) 404207-MP Completed unit, matte finish, 220 Volt, Multi-Platform
configuration;


4.) 404207-B Completed unit, matte finish, 220 Volt;



5.) 404207-USAB Completed unit, matte finish, 220 Volt, USA-style power cord;



6.) 404208-B Completed unit, matte finish, 110 Volt; and



7.) 404208-MP Completed unit, matte finish, 110 Volt, Multi-Platform
configuration.

The NannoLight Intense Pulsed Light System is indicated for use in surgical, aesthetic and cosmetic applications requiring selective photothermolysis (photocoagulation or coagulation) and hemostasis of soft tissue in the medical specialties of general and plastic surgery and dermatology.



Code Information Serial Numbers:   272102 280103 280104 280105 280901 281004 280810 280506 280509 280609 280808 280809 281304 280801 280206 280301 280306 280207 280402 280702 280703 280403 280405 280701 280701 280706 280210 280303 280805 280802 280108 280208 280302 280508 280604 280906 280908 280909 280910 281001 280804 280905 280209 280803 280409 280510 280610 280401 280709 280806 280708 280307 280807 280904 281005 280902 280304 280503 280507 and 281204.  Serial numbers sumbitted 4/22/09.
Recalling Firm/
Manufacturer		 Sybaritic, Inc
9220 James Ave S
Bloomington MN 55431-2302
For Additional Information Contact
952-888-8282
Manufacturer Reason
for Recall		 Sybaritic Inc. had an issue with the 585nm filter used with the NannoLight MP50. The filter may cause unwanted burning and should not be used for vascular lesion treatments.
FDA Determined
Cause 2		 Device Design
Action A "Sybaritic" notification letter dated April 15, 2008 was issued to consignees. The letter described the modifications to the protocols for the NannoLight MP50 and the temporary replacement of 585 Filter for the 560 Filter for Vascular Lesions until further notice. They requested the immediate use of the protocols replacing all other versions. A follow-up letter dated June 3, 2008 was issued to customers. The letter included an attachment " Product Notice Nannolight MP50 585 nm "special" filter from Sybaritic, Inc. The letter described the new 585 nm "bandwidth filter". Also the notification advised consignees to discontinue the use of the old 585 filter and to use 560nm filter until they receive the new 585 nm bandwidth filter. Please direct any questions to your Account Manager or to Sybaritic, Inc. by calling 1-800-445-8418 or 1-952-888-8282.
Quantity in Commerce 59
Distribution Worldwide Distribution -- US (states of WA, CA, MN, FL and AR), POLAND, THAILAND, CHILE, CANADA, KOREA, AZERBAIJAN, INDIA, SPAIN, ARGENTINA, RUSSIA, GREECE, PHILIPPINES, POLAND, INDIA, JORDAN, TURKEY, MEXICO, URUGUAY,BELGIUM, LEBANON, BULGARIA and SINGAPORE.
Total Product Life Cycle TPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = GEX and Original Applicant = GLOBAL USA DISTRIBUTION, LLC.
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