FDA recall record

Canadian Art Prints UPC Code 772665860083, Stock code PLT008, Indigenous recall — FDA F-1515-2024

Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).

Class IIclassification
F-1515-2024official record ID
Jul 31, 2024report date

Recall record at a glance

Official recordF-1515-2024
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCanadian Art Prints
Report dateJul 31, 2024
Recall initiation dateJun 28, 2024
Quantity301 sets distributed in the US
LocationRichmond, British Columbia, Canada

Official product description

UPC Code 772665860083, Stock code PLT008, Indigenous Collection Signature Plates set - Not Forgotten & Ancient Messages. Artist Maxine Noel on box and back of plates. Brand Indigenous Collection by CAP on box and back of plates. Not Forgotten is an image of a woman with indigenous iconography in her dress in blues, reds and creams. There are spirits in the background. Ancient Messages is an image with a woman holding her arm upward with indigenous patterns in her dress in greens and oranges

Why the product was recalled

Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).

Distribution information

Distributed in AK, AZ, CA, GA, ID, IL, MI, NC, NM, NY, OR, PA, SC, SD, TX, UT, WA, and WI.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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