Sperti™ Vitamin D Lamp May 6, 2026 · Published by Health Canada · Official notice
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Alert type : Health product recall
Category : Health products - Medical devices - General and plastic surgery
Product : Sperti™ Vitamin D Lamp
Issue : Medical devices - Unauthorised device
What to do : Customers to be notified by the manufacturer. Instructions to be provded.
Audience : General public
Recall class : Type II
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Affected products Lot or serial number Model or catalogue number Sperti™ Vitamin D Lamp Not applicable. DUV-4F
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.