Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 12, 2025 (1 years ago)

Outer carton labeled 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 allergens (almonds).

Undeclared allergen: Tree nuts

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

Outer carton labeled: "Cookie Butter Banana Pie" Inner carton labeled: "Tropical Key Lime Pie" Product contained inside: "Cookie Butter Banana Pie" NET WT. 11 LB 2.8 OZ (5.06 kg) GROSS WT: 12.96 LB (5.88 kg)

Quantity: 1191 cases (2 units per case)

Food: Milk & dairy 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.

SKU #8495241471 Lot #6Z4L04 UPC: 767367101855 Expiration Date: 11/04/2025

Where it was sold

California Florida Iowa Illinois Kansas Minnesota Mississippi North Carolina New Jersey Nevada New York Oklahoma South Carolina Tennessee Texas Washington

FDA's distribution note: IL, OK, NJ, SC, NY, CA, NC, WA, IA, MS, KS, FL, TN, NV, TX, MN

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 tree nuts; 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
Apr 12, 2025
In FDA report of
May 7, 2025
Terminated
Aug 8, 2025
FDA recall number
F-0748-2025 · event 96704
Official record
FDA enforcement report search

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