Distribuidora La Casa Grande
FDA import alert and refusal historySan Pedro,Santiago,N.L.Mexico., MexicoFEI 3003967495
As of October 26, 2026, Distribuidora La Casa Grande (San Pedro,Santiago,N.L.Mexico., Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for charal enchilado/fried fish with chilli pepper, published by FDA on June 26, 2018, 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 16-81 · 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 Distribuidora La Casa Grande
2 records, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 16-81red listCharal Enchilado/Fried Fish with Chilli PepperSource
2009
- Import alert listingListed on Import Alert 45-02red listChurritos de Maiz con Chili Corn SticksSource
Questions about Distribuidora La Casa Grande
- Is Distribuidora La Casa Grande on an FDA import alert?
- Yes. As of October 26, 2026, Distribuidora La Casa Grande is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for charal enchilado/fried fish with chilli pepper; FDA published the listing on June 26, 2018.
- Has FDA refused shipments from Distribuidora La Casa Grande?
- No FDA import refusals for Distribuidora La Casa Grande appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Distribuidora La Casa Grande's FEI number?
- Distribuidora La Casa Grande's FDA Establishment Identifier (FEI) is 3003967495.
- Can shipments from Distribuidora La Casa Grande still enter the U.S.?
- Shipments of charal enchilado/fried fish with chilli pepper from Distribuidora La Casa Grande can be detained without physical examination under Import Alert 16-81; 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.