Food Recall Check
Class I · High risk Terminated Initiated Nov 21, 2025 (11 months ago)

Choceur Cookie Butter Holiday Bark recall

Recalled by Silvestri Sweets Inc dba Carousel Candies · Geneva, IL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared pecan

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

Choceur Cookie Butter Holiday Bark. Standup Pouch Bag. 5 oz. (142g). UPC: 4069365095690. Wholesale unit is split case, with 9 of each item per case.

Quantity: 134,865 bags

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.

Lot #: 29225 Best By 05/2026 Lot #: 28525  Best By 05/2026 Lot #: 29925  Best By 05/2026 Lot #: 30625  Best By 06/2026

Where it was sold

Nationwide.

FDA's distribution note: The recalled items were distributed nationwide through Aldi grocery stores.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Silvestri Sweets Inc dba Carousel Candies
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 21, 2025
In FDA report of
Dec 31, 2025
Terminated
Jan 29, 2026
FDA recall number
H-0339-2026 · event 98067
Official record
FDA enforcement report search

Also recalled with it (1 more product)

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

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