Urban Outfitters Inc. Recall: Elevated levels of cadmium in plates
United States
TerminatedClass II
- Company
- Urban Outfitters Inc.
- Product
- Elin Dessert Plates. The recalled plates are lilac in color…
- Recall date
- July 11, 2024
- Terminated
- April 11, 2025
- Source
- FDA
Reason for recall
Elevated levels of cadmium in plates
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Elin Dessert Plates. The recalled plates are lilac in color with orange mushroom, moth, and fern motifs. The plates measure 21 cm (8.25 inches) in diameter and have scalloped edges. Plates sold individually in store. | Not published in this source record | 3,757 units | n/a |
Distribution
- Distributed nationwide.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1738-2024
- Event ID
- 94957
- Status
- Terminated
- Classification
- Class II
- Company
- Urban Outfitters Inc.
- Product description
- Elin Dessert Plates. The recalled plates are lilac in color with orange mushroom, moth, and fern motifs. The plates measure 21 cm (8.25 inches) in diameter and have scalloped edges. Plates sold individually in store.
- Quantity
- 3,757 units
- Reason
- Elevated levels of cadmium in plates
- Recall initiation date
- July 11, 2024
- Report date
- August 7, 2024
- Classification date
- Not published in this source record
- Termination date
- April 11, 2025
- Distribution pattern
- Distributed nationwide.
- UPC, lot, and code information
- n/a
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Urban Outfitters Inc.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
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. Read the full medical disclaimer.
