Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit, UPC: 0070896117274, total weight 28.7oz
Summary
The FDA issued a Class II for Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit, UPC: 0070896117274, tota by Wilton Industries Inc. Reason: Milk is missing from the product's allergen Contains statement.
Details
Source
Food Recall
External ID
F-0994-2022
Action Date
2022-04-20
Status
Terminated
Category
food
Product Description
Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit, UPC: 0070896117274, total weight 28.7oz
Lot/Code Info: Lots 22005, 22006 and 22007
Quantity Affected: 41,256 units
Reason for Recall
Milk is missing from the product's allergen Contains statement
Distribution
Nationwide US. Colombia.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-24
Company
Naperville, IL
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 40 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Wilton Industries Inc has 3 FDA actions in our database, including 3 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 (Wilton Industries Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wilton Industries Inc have FDA actions?
Wilton Industries Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0994-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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