Kapulsky
FDA import alert and refusal historyNetanya, IsraelFEI 3008938555
As of October 25, 2026, Kapulsky (Netanya, Israel) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for cake (black forest torte); cakes chocolate party cake; cakes (black forest torte), published by FDA on October 2, 2015, is also listed on Import Alert 45-02 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red listIA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kapulsky
2 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-39red listCake (Black Forest Torte); Cakes Chocolate Party Cake; Cakes (Black Forest Torte)Source
2011
- Import alert listingListed on Import Alert 45-02red listChocolate Cake (Party); Chocolate Cake (Coated Torte); Cake,Custard or Cream Filled; Chocolate Cake (Black Forest Torte); Cake Without Custard or Cream Filling; Chocolate cake (Heart-Shaped); Cakes, filled (other than fruit or jelly)Source
Questions about Kapulsky
- Is Kapulsky on an FDA import alert?
- Yes. As of October 25, 2026, Kapulsky is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for cake (black forest torte); cakes chocolate party cake; cakes (black forest torte); FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Kapulsky?
- No FDA import refusals for Kapulsky appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Kapulsky's FEI number?
- Kapulsky's FDA Establishment Identifier (FEI) is 3008938555.
- Can shipments from Kapulsky still enter the U.S.?
- Shipments of cake (black forest torte); cakes chocolate party cake; cakes (black forest torte) from Kapulsky can be detained without physical examination under Import Alert 99-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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