Sperti™ Vitamin D Lamp
Sperti™ Vitamin D Lamp Recall Summary The Sperti™ Vitamin D Lamp is being recalled in Canada because it is an unauthorized medical device that has not been approved by Health Canada for sale. The lamp was distributed across Canada. This is classified as a Class II recall, which means the product could cause temporary or medically reversible adverse effects.
- Product
- Sperti™ Vitamin D Lamp
- Reason
- Unauthorised device
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-05-06
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/78246ca7-3752-4cc0-b161-d80ac2677aa4