Food Recall Check
Class II · Moderate risk Terminated Initiated May 16, 2025 (17 months ago)

1) Madeline's Patisserie recall

Recalled by Element 112, LLC · Sylvania, OH, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared wheat

Undeclared allergen: Wheat

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

1) Madeline's Patisserie 2.5 ounce Chocolate Croissant, Net Wt. 3 lbs. 8 oz. (1,587.6g), packaged in a food safe polypropylene bag and packed in a food service case; 24 per case 2) Madeline's Patisserie 3.5 ounce Chocolate Croissant, Net Wt. 4 lbs. 11 oz. (2,126.2g), packaged in a food safe polypropylene bag and packed in a food service case; 24 per case

Quantity: 1) 198 cases; 2) 106 cases (304 cases TOTAL)

Food: Chocolate & candy

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

1) UPC: 196852079797; SKU: CR-CH-01; Lot codes: 0E0BBE, 0E0GBE, 0DC0BE, 0DBDBE, 0BAHBE, 0D0HBE, 0CBEBE, 0CACBE, 0C0FBE, 0C0GBE 2) UPC: 196852976959; SKU: CR-CH-02; Lot codes: 0DBCBE, 0CBEBE, 0CAGBE, 0CAHBE, 0BBGBE, 0CAABE

Where it was sold

Michigan Ohio

FDA's distribution note: Four (4) distributors in: MI, OH

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Element 112, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
May 16, 2025
In FDA report of
Jul 2, 2025
Terminated
Sep 10, 2025
FDA recall number
H-0058-2025 · event 96901
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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