Elin Dessert Plates. The recalled plates are lilac in color with orange mushroom, moth, and fern motifs. The plates meas
Summary
The FDA issued a Class II for Elin Dessert Plates. The recalled plates are lilac in color with orange mushroom by Urban Outfitters Inc.. Reason: Elevated levels of cadmium in plates.
Details
Source
Food Recall
External ID
F-1738-2024
Action Date
2024-08-07
Status
Terminated
Category
food
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.
Lot/Code Info: n/a
Quantity Affected: 3,757 units
Reason for Recall
Elevated levels of cadmium in plates
Distribution
Distributed nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-11
Company
Philadelphia, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 105 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Urban Outfitters Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Urban Outfitters Inc. have FDA actions?
This is the only FDA action we have on record for Urban Outfitters Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1738-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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