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Sperti™ vitamin d lamp

Official notice

6 May 2026

MediumHealth Canada

An official Health Canada notice concerns Sperti™ vitamin d lamp. 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. Published 2026-05-06.

What to do now

Customers to be notified by the manufacturer. Instructions to be provded.

Recall number

82036

Official notice

2026-05-06

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.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Skus

DUV-4F

Other

RA RA-82036

Model Numbers

DUV-4F

Recall Numbers

82036

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Affected products

Product 1

Lot or serial number - Not applicable., Model or catalogue number - DUV-4F

Risk / 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.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Kbd Sperti Sunlamps, Fabtech Shanghai.

Source & status

Source

Health Canada

Tier

beta

Category

HOME

Classification

Type II

App estimate

medium

Recall details

Recall number

82036

Classification

Type II

Source tier

beta

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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