Alicia Alvarez Gutierres
FDA import alert and refusal historyGuadalajara, MexicoFEI 3010013637
As of October 26, 2026, Alicia Alvarez Gutierres (Guadalajara, Mexico) is on the red list of FDA Import Alert 99-42 (Foods: heavy metal (toxic element) contamination) for dried prunes, published by FDA on October 13, 2022, is also listed on Import Alert 99-39 (red list) and Import Alert 45-02 (red list) and Import Alert 99-19 (red list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Alicia Alvarez Gutierres
4 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-42red listDried PrunesSource
2015
- Import alert listingListed on Import Alert 99-39red listBrown SugarSource
2012
- Import alert listingListed on Import Alert 45-02red listChorizo Mix SeasoningSource
2009
- Import alert listingListed on Import Alert 99-19red listPumpkin Seed (Edible Seed)Source
Questions about Alicia Alvarez Gutierres
- Is Alicia Alvarez Gutierres on an FDA import alert?
- Yes. As of October 26, 2026, Alicia Alvarez Gutierres is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for dried prunes; FDA published the listing on October 13, 2022.
- Has FDA refused shipments from Alicia Alvarez Gutierres?
- No FDA import refusals for Alicia Alvarez Gutierres appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Alicia Alvarez Gutierres's FEI number?
- Alicia Alvarez Gutierres's FDA Establishment Identifier (FEI) is 3010013637.
- Can shipments from Alicia Alvarez Gutierres still enter the U.S.?
- Shipments of dried prunes from Alicia Alvarez Gutierres can be detained without physical examination under Import Alert 99-42; 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.