Maria De Lourdes Sanchez Arreola
FDA import alert and refusal historyEl Salto, MexicoFEI 3012290856
As of October 26, 2026, Maria De Lourdes Sanchez Arreola (El Salto, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft candy lollipop, published by FDA on December 10, 2024, 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
- None on record
Every FDA record for Maria De Lourdes Sanchez Arreola
1 record, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 45-02red listSoft Candy LollipopSource
Questions about Maria De Lourdes Sanchez Arreola
- Is Maria De Lourdes Sanchez Arreola on an FDA import alert?
- Yes. As of October 26, 2026, Maria De Lourdes Sanchez Arreola is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft candy lollipop; FDA published the listing on December 10, 2024.
- Has FDA refused shipments from Maria De Lourdes Sanchez Arreola?
- No FDA import refusals for Maria De Lourdes Sanchez Arreola appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Maria De Lourdes Sanchez Arreola's FEI number?
- Maria De Lourdes Sanchez Arreola's FDA Establishment Identifier (FEI) is 3012290856.
- Can shipments from Maria De Lourdes Sanchez Arreola still enter the U.S.?
- Shipments of soft candy lollipop from Maria De Lourdes Sanchez Arreola 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).
Buying from Maria De Lourdes Sanchez Arreola?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.