Madeline's Patisserie 4.25 Inch Butter Croissant Bun, Net Wt. 4 lbs. 6 oz (1,984.47 g), packaged in a food safe polyprop
Summary
The FDA issued a Class II for Madeline's Patisserie 4.25 Inch Butter Croissant Bun, Net Wt. 4 lbs. 6 oz (1,984 by Element 112, LLC. Reason: Undeclared wheat.
Details
Source
Food Recall
External ID
H-0060-2025
Action Date
2025-07-02
Status
Terminated
Category
food
Product Description
Madeline's Patisserie 4.25 Inch Butter Croissant Bun, Net Wt. 4 lbs. 6 oz (1,984.47 g), packaged in a food safe polypropylene bag and packed in a food service case; 24 per case
Lot/Code Info: UPC: 196852170685; SKU: CR-BN-01; Lot codes: 0E0FBE, 0DBDBE, 0BAHBE, 0DAGBE, 0D0GBE, 0D0DBE, 0DAABE, 0D0CBE, 0CBFBE, 0CBEBE, 0CB0BE, 102524JB, 0CADBE, 0BBFBE
Quantity Affected: 276 cases
Reason for Recall
Undeclared wheat
Distribution
Four (4) distributors in: MI, OH
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-16
Company
Sylvania, OH
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 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Element 112, LLC 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 (Element 112, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Element 112, LLC have FDA actions?
Element 112, LLC 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 "H-0060-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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