Skip to main content
High RiskFDAfda-F-1515-2024CHEMICAL EXPOSURE

UPC Code 772665860083, Stock code PLT008, Indigenous Collection Signature Plates set - Not Forgotten & Ancient Messages. Artist Maxine No...

Category
Units Affected
301
Recall Date
June 28, 2024
Issuing Agency
Hazard
Chemical Exposure

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1515-2024.

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

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1515-2024.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Canadian Art Prints or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1515-2024.

Canadian Art Prints

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Canadian Art Prints Recall FAQ

Canadian Art Prints is the subject of a food safety report: UPC Code 772665860083, Stock code PLT008, Indigenous Collection Signature Plates set - Not Forgotten & Ancient Messages. Artist Maxine No.... The notice was published on June 28, 2024 by the U.S. Food and Drug Administration (FDA). Approximately 301 units are potentially affected.