Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 18, 2023 (3 years ago)

Sienna Bakery Chocolate Decadent Brownies recall

Recalled by Dianne's Fine Desserts · Newburyport, MA, United States

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

Why it was recalled

Contains undeclared peanuts.

Undeclared allergen: Peanut

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

Sienna Bakery Chocolate Decadent Brownies (Tray)

Quantity: 512 cases

Food: Chocolate & candy Bread & bakery

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.

Trays are labeled as Sienna Bakery Chocolate Decadent Brownies (GFS#226240) with lot code of 23243 printed on the bottom right corner of the tray (picture attached). Tray size is 16.5 x 12.5. x 2 inches Outer cardboard case is labeled Sienna Bakery Chocolate Peanut Butter Brownies. Case label that contains the Lot code 6Z3H31 and 23243

Where it was sold

Arkansas Florida Illinois Indiana Kentucky Michigan Missouri New York Ohio Pennsylvania South Carolina Tennessee Wisconsin West Virginia

FDA's distribution note: AR, FL, IL, IN, KY, MI, MO, NY, OH, PA, SC, TN, WI, WV

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 peanut; 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
Dianne's Fine Desserts
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 18, 2023
In FDA report of
Dec 20, 2023
Terminated
Jul 16, 2024
FDA recall number
F-0580-2024 · event 93468
Official record
FDA enforcement report search

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