| Class 3 Device Recall Dermalight 80, UVB083 | |
Date Initiated by Firm | April 08, 2013 |
Date Posted | July 19, 2013 |
Recall Status1 |
Terminated 3 on February 24, 2014 |
Recall Number | Z-1779-2013 |
Recall Event ID |
65494 |
510(K)Number | K903660 |
Product Classification |
Lamp, infrared, non heating - Product Code FTC
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Product | Dermalight 80 Model Number UVB-083, one unit per box.
The Dermalight 80 is a Phototherapy light unit that provides ultraviolet radiation therapy for diagnosed skin disorders such as Psoriasis and Vitiligo. |
Code Information |
The following batch and serial numbers are affected by the recall: Batch 007778, Serial numbers D83-30016 to D83-30021. |
Recalling Firm/ Manufacturer |
National Biological Corp 23700 Mercantile Rd Beachwood OH 44122-5900
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For Additional Information Contact | 216-831-0600 |
Manufacturer Reason for Recall | The incorrect manual may have been packaged with this product. UVB-083 devices may have included the
manual for a UVA-080 device. |
FDA Determined Cause 2 | Labeling mix-ups |
Action | The firm, National Biological, sent an "VOLUNTARY PRODUCT RECALL NOTIFICATION" letter dated May 10, 2013 to its consignees/customers by UPS or other delivery service with a signature required. The letter described the product, problem and actions to be taken. Consignees/customers who do not respond to the letter will be contacted via telephone. The customers were instructed to check within your household to determine if you have any of the listed product; immediately destroy the incorrect User Manual, it is not necessary to return the product; record the Customer Name and or the Dermalight-80 serial number and complete and return the enclosed Verification Form, even if you do not have any User Manuals to destroy.
Please contact your National Biological Corporation sales representative if you have any questions regarding this recall, any of our products, or would like assistance with the recall call 216-831-0600 or 800-338-5045 email: infor@PhototherapyExperts.com. |
Quantity in Commerce | 6 units |
Distribution | US distribution including the states of: AL, CA, MN, and NC. |
Total Product Life Cycle | TPLC Device Report |
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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.
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510(K) Database | 510(K)s with Product Code = FTC
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