Sperti Vitamin D Lamp Recall
Areazine synthesizes this Health Canada recall directly from Health Canada's official public data feed. See our methodology for full source attribution and refresh cadence.
Health Canada has issued a recall for the Sperti Vitamin D Lamp because it lacks the required medical device licence for sale in Canada.
What this Health Canada recall tells you, and what most readers miss
This notice was issued by Health Canada on May 6, 2026 and geographically references Canada. Its severity classification of "low" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - Product & Food Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, health-canada, health-product.
What Happened
The Sperti™ Vitamin D Lamp is being recalled because it requires a medical device licence to be sold in Canada, but an internal review confirmed it was not licensed.
Which Products Are Affected
The affected product is the Sperti™ Vitamin D Lamp with model number DUV-4F. Lot or serial number is not applicable.
What You Should Do
Consumers should refer to the recall notice from Health Canada for guidance, as specific actions such as returns or refunds are not detailed in the available information.
Why This Matters
This recall highlights the importance of regulatory compliance for medical devices to ensure they meet safety standards in Canada, potentially protecting public health from unlicensed products.
Source
This information is from Health Canada. For more details, visit: https://recalls-rappels.canada.ca/en/alert-recall/spertitm-vitamin-lamp
Original source: Health Canada Official Notice ↗
Related Product & Food Recalls
All Product & Food Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this Health Canada recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (888 characters here).
Similar severity timing
Same severity (low) notices issued closest in time to May 6, 2026.
Frequently Asked Questions
Common questions about this Health Canada recall.