Sperti™ Vitamin D Lamp
Last updated
Summary
Product
Sperti™ Vitamin D Lamp
Issue
Medical devices - Unauthorised device
What to do
Customers to be notified by the manufacturer. Instructions to be provded.
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Sperti™ Vitamin D Lamp | Not applicable. | DUV-4F |
Issue
The Sperti™ Vitamin D lamp requires a medical device licence to be sold in Canada. An internal review confirmed this device was not licensed for sale in Canada.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General and plastic surgery
Companies
Kbd, Inc./ Sperti Sunlamps
4208 W Cheyenne Ave #120, North Las Vegas, Nevada, United States, 89032
Global Fabtech Shanghai, Ltd
No. 318 Tianfu Road, Jiuting, Shanghai, China, 201615
Published by
Health Canada
Audience
General public
Recall class
Type II
Recall date
Identification number
RA-82036
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