Azucares Dulces Produce
FDA import alert and refusal historyMartinez De La Torre, MexicoFEI 3006366948
Recorded by FDA as AZUCARES DULCES PRODUCE
As of October 26, 2026, Azucares Dulces Produce (Martinez De La Torre, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for assorted hard candy dulces mexicanos colacions, published by FDA on September 18, 2009, is also listed on Import Alert 99-05 (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 45-02 · red listIA 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Azucares Dulces Produce
2 records, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listassorted hard candy Dulces Mexicanos ColacionsSource
- Import alert listingListed on Import Alert 99-05red listPapaya (Papaw) (Subtropical and Tropical Fruit), Raw, Fresh, Ambient; Papaya (Papaw) (Subtropical and Tropical Fruit), Raw, Fresh, RefrigeratedSource
Questions about Azucares Dulces Produce
- Is Azucares Dulces Produce on an FDA import alert?
- Yes. As of October 26, 2026, Azucares Dulces Produce is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for assorted hard candy dulces mexicanos colacions; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Azucares Dulces Produce?
- No FDA import refusals for Azucares Dulces Produce appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Azucares Dulces Produce's FEI number?
- Azucares Dulces Produce's FDA Establishment Identifier (FEI) is 3006366948.
- Can shipments from Azucares Dulces Produce still enter the U.S.?
- Shipments of assorted hard candy dulces mexicanos colacions from Azucares Dulces Produce 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.