Quick summary: Sperti™ Vitamin D Lamp. Reason: Unauthorised device. Category: General and plastic surgery. Date: 2026-05-06.
Sperti™ Vitamin D Lamp
2026-05-06
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Sperti™ Vitamin D Lamp. Reason: Unauthorised device. Category: General and plastic surgery. Date: 2026-05-06.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
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.
What you should do
- Customers to be notified by the manufacturer. Instructions to be provded.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
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