Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g) UPC:4056489365365 Product packaged in a cardboard/plastic
Summary
The FDA issued a Class II for Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g) UPC:4056489365365 by Lidl US TRADING. Reason: Undeclared Wheat, Soy, Egg, Milk, Tree Nuts (foreign language labeling).
Details
Source
Food Recall
External ID
F-1148-2024
Action Date
2024-04-17
Status
Terminated
Category
food
Product Description
Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g) UPC:4056489365365 Product packaged in a cardboard/plastic container
Lot/Code Info: Expiration date:Jan-22-2025 Batch Number L34723B1
Quantity Affected: 1,792 units
Reason for Recall
Undeclared Wheat, Soy, Egg, Milk, Tree Nuts (foreign language labeling)
Distribution
Imported product directly shipped to a warehouse in Virginia and then distributed to 3 distribution centers in North Carolina, Virginia, and Maryland. From the distribution centers distributed to Lidl retail stores in Delaware, District of Columbia, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-03-28
Company
Arlington, VA
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 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lidl US TRADING has 15 FDA actions in our database, including 15 recalls.
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 (Lidl US TRADING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lidl US TRADING have FDA actions?
Lidl US TRADING has 15 FDA actions in our database, including 15 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1148-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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