FDA recall record

Canadian Art Prints Tranquility & Teachings William Monague plate set, brand recall — FDA F-1175-2024

Product has been recalled because it may exceed FDA guidance levels for leachable lead.

Class IIclassification
F-1175-2024official record ID
Apr 24, 2024report date

Recall record at a glance

Official recordF-1175-2024
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmCanadian Art Prints
Report dateApr 24, 2024
Recall initiation dateMar 11, 2024
Quantity83 boxes (2 plates per box) distributed in the US
LocationRichmond, British Columbia, Canada

Official product description

Tranquility & Teachings William Monague plate set, brand Indigenous Collection by CAP. Each box consists of two plates, each plate is 7.5inch. Stock code PLT015, UPC 772665860151. Tranquility plate #1 artwork is observed with a lakeside landscape at night in blues and greens with an eagle and moon in the night sky and 3 turtles and bullrushes in the foreground. Teachings plate #2 artwork is observed with a lakeside landscape at night in blues and greens with a large moon in the sky and a glowing tipi with people inside in the midground.

Why the product was recalled

Product has been recalled because it may exceed FDA guidance levels for leachable lead.

Distribution information

Plates were distributed in Canada and in the United States (AR, AZ, CA, FL HI, IN, KS, MT, NY, OR, SC, SD, 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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