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El Camaron Sinaloense

FDA import alert and refusal historyTijuana, MexicoFEI 3001799084

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Example subjectEl Camaron Sinaloens added to Import Alert 16-129 (red list)

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As of October 25, 2026, El Camaron Sinaloense (Tijuana, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for snails, aquatic, other aquatic species; raw sea snail, published by FDA on September 18, 2009, 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 El Camaron Sinaloense

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listSnails, Aquatic, Other Aquatic Species; Raw sea snail
    Source

Questions about El Camaron Sinaloense

Is El Camaron Sinaloense on an FDA import alert?
Yes. As of October 25, 2026, El Camaron Sinaloense is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for snails, aquatic, other aquatic species; raw sea snail; FDA published the listing on September 18, 2009.
Has FDA refused shipments from El Camaron Sinaloense?
No FDA import refusals for El Camaron Sinaloense appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is El Camaron Sinaloense's FEI number?
El Camaron Sinaloense's FDA Establishment Identifier (FEI) is 3001799084.
Can shipments from El Camaron Sinaloense still enter the U.S.?
Shipments of snails, aquatic, other aquatic species; raw sea snail from El Camaron Sinaloense 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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Example subjectEl Camaron Sinaloens added to Import Alert 16-129 (red list)

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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.