CanadaSperti™ Vitamin D Lamp (model DUV-4F) sold under KBD, Inc./Sperti Sunlamps and made by Global Fabtech Shanghai is affected; model/catalogue number DUV-4F identifies the product. It was recalled because it requires a medical device licence to be sold in Canada and the device was not licensed for sale in Canada; customers will be notified by the manufacturer and instructions will be provided.
What's being recalled
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.
How to identify it
Affected products: Sperti™ Vitamin D Lamp; Lot or serial number: Not applicable.; Model or catalogue number: DUV-4F
The hazard
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.
What to do
Customers to be notified by the manufacturer. Instructions to be provded.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)