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Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
- Recall initiated
- Reported by source
- Recall terminated
Recalled products
Product description
UPC
Quantity
Lot / code information
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.
772665860106
161 sets distributed in the U.S
Stock Code PLT010
Distribution
Distributed in AK
AZ
CA
GA
ID
IL
MI
NC
NM
NY
OR
PA
SC
SD
TX
UT
WA
and WI.
Official source record
Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1516-2024
Event ID
94880
Status
Terminated
Classification
Class II
Company
Canadian Art Prints
Product 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.
Quantity
161 sets distributed in the U.S
Reason
Glazed ceramic plates are recalled because they may exceed FDA guidance levels for leachable lead (3.0mg/L).
Recall initiation date
June 28, 2024
Report date
July 31, 2024
Classification date
Not published in this source record
Termination date
March 25, 2025
Distribution pattern
Distributed in AK, AZ, CA, GA, ID, IL, MI, NC, NM, NY, OR, PA, SC, SD, TX, UT, WA, and WI.
UPC, lot, and code information
UPC 772665860106; Stock Code PLT010
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 94880 with 1 other product
entry in Public Health Trace.
FDA Recall🇺🇸 United StatesTerminatedTerminated: March 25, 2025Historical recordClass II
A map highlighting the states named in the source's distribution description.
Distributed
No data published
Shading reflects state-level totals only, as published by the source. It does not imply
county-level or point-level precision.
Distribution map
State
Distributed
Alaska
1
Arizona
1
California
1
Georgia
1
Idaho
1
Illinois
1
Michigan
1
North Carolina
1
New Mexico
1
New York
1
Oregon
1
Pennsylvania
1
South Carolina
1
South Dakota
1
Texas
1
Utah
1
Washington
1
Wisconsin
1
States shown are extracted from the source's free-text distribution description above; a narrative
description (e.g. "distributed nationwide") may not list individual states to extract.
View raw source data
-- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company
or product is unsafe beyond what the official source has published.
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