UPC 772665860106. PLT010. Indigenous Collection Signature Plates set - Dancing Bears & Three Bears on box and back of plate. Art by Dawn Oman. Brand Indigenous Collection by CAP on box and back of plate. The Dancing Bears is a scene with three dancing polar bears with a night sky under the aurora borealis with falling snow. Three Bears shows three polar bears walking in a line with a colorful sky and land and snow is falling.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Stock Code PLT010
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Canadian Art Prints
- Reason for Recall:
- Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
UPC 772665860106. PLT010. Indigenous Collection Signature Plates set - Dancing Bears & Three Bears on box and back of plate. Art by Dawn Oman. Brand Indigenous Collection by CAP on box and back of plate. The Dancing Bears is a scene with three dancing polar bears with a night sky under the aurora borealis with falling snow. Three Bears shows three polar bears walking in a line with a colorful sky and land and snow is falling.
Product Codes/Lot Numbers:
Stock Code PLT010
Distribution:
Distributed in: AK, AZ, CA, GA, ID, IL, MI, NC, NM, NY, OR, PA, SC, SD, TX, UT, WA, WI
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-1516-2024
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