CLASS I Food recall · Reported 8 Jan 2025 · FDA Enforcement Report

Napoleonas Torte packaged under the following sizes: Small recalled

Lithuanian Bakery is recalling Napoleonas Torte packaged under the following sizes: Small, distributed in 7 states. The recall was initiated on 1 Nov 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesNot provided
Quantity recalled120 packages (1.25lb containers), 30 packages (2.75lb containers)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0319-2025
FDA event ID
95667
Recalling firm
Lithuanian Bakery, Omaha, NE
Classification
Class I
Status
Terminated
Recall initiated
1 Nov 2024
FDA classified
30 Dec 2024
Reported
8 Jan 2025
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Milk

Timeline

1 Nov 2024Recall initiated by company
30 Dec 2024Classified by FDA+59 days
8 Jan 2025Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Products contain undeclared allergens (milk, soy, and wheat) and undeclared sulfites, yellow 5, yellow 6.

Product as listed by the FDA

Napoleonas Torte packaged under the following sizes: 1. Small, Net Wt 1.25 lbs. (sub ingredients contain wheat, yellow #5 and #6, and sulfites not declared on final product label) 2. Medium, Net Wt 2.75 lbs. (sub ingredients contain yellow #5 and #6 not declared on final product label) 3. Large, Net Wt 6 lbs (sub ingredients contain wheat, milk, yellow #5 and #6, and sulfites not declared on final product label)

Where it was distributed

Distributed to store front customers at retail stores in IA, IL, KS, MO, MN, NE, and SD.

IowaIllinoisKansasMinnesotaMissouriNebraskaSouth Dakota

Questions about this recall

Why was it recalled?

Products contain undeclared allergens (milk, soy, and wheat) and undeclared sulfites, yellow 5, yellow 6.

Which lots are affected?

Not provided

Where was it sold?

Distributed to store front customers at retail stores in IA, IL, KS, MO, MN, NE, and SD.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 95667

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