Kidskan SA de CV
FDA import alert and refusal historySanta Catarina, MexicoFEI 3010122135
Recorded by FDA as KIDSKAN SA DE CV
As of October 26, 2026, Kidskan SA de CV (Santa Catarina, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for mini orange unicorn lollipop (paleta mini unicornio naranja), published by FDA on February 26, 2016, 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 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Kidskan SA de CV
2 records, newest first. Each line links to the FDA page it came from.
2023
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2016
- Import alert listingListed on Import Alert 45-02red listMini Orange Unicorn Lollipop (Paleta Mini Unicornio Naranja)Source
Questions about Kidskan SA de CV
- Is Kidskan SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Kidskan SA de CV is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for mini orange unicorn lollipop (paleta mini unicornio naranja); FDA published the listing on February 26, 2016.
- Has FDA refused shipments from Kidskan SA de CV?
- No FDA import refusals for Kidskan SA de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Kidskan SA de CV last inspected by FDA?
- FDA's most recent inspection of Kidskan SA de CV with a final classification is dated August 23, 2023 and was classified VAI (Voluntary Action Indicated).
- What is Kidskan SA de CV's FEI number?
- Kidskan SA de CV's FDA Establishment Identifier (FEI) is 3010122135.
- Can shipments from Kidskan SA de CV still enter the U.S.?
- Shipments of mini orange unicorn lollipop (paleta mini unicornio naranja) from Kidskan SA de CV can be detained without physical examination under Import Alert 45-02; 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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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.