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Hul Kin, S.A. De C.V.

FDA import alert and refusal historyDzilam De Bravo, Yucatan Merida, MexicoFEI 3010263062

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Example subjectHul Kin, S.A. De C.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Hul Kin, S.A. De C.V. (Dzilam De Bravo, Yucatan Merida, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for blue crab, published by FDA on July 21, 2017, and has 1 FDA import refusal recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Crab · SALMONELLA
Last warning letter
None found
Last inspection
None on record

Every FDA record for Hul Kin, S.A. De C.V.

2 records, newest first. Each line links to the FDA page it came from.

2017

  1. Import alert listing
    Listed on Import Alert 16-81red listBlue Crab
    Source
  2. Import refusal
    Refused, CrabSALMONELLAEntry EJ7-0107283-0
    Source

Refusal charges, in plain English

  • SALMONELLA1 refused line

    Salmonella

    The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Hul Kin, S.A. De C.V.

Is Hul Kin, S.A. De C.V. on an FDA import alert?
Yes. As of October 26, 2026, Hul Kin, S.A. De C.V. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for blue crab; FDA published the listing on July 21, 2017.
Has FDA refused shipments from Hul Kin, S.A. De C.V.?
Yes. FDA refused 1 shipment line from Hul Kin, S.A. De C.V. on July 20, 2017. The most recent, on July 20, 2017, was crab, charged as SALMONELLA (salmonella).
Why did FDA refuse Hul Kin, S.A. De C.V.'s shipments?
The most frequent charge is SALMONELLA (salmonella, 1 line).
What is Hul Kin, S.A. De C.V.'s FEI number?
Hul Kin, S.A. De C.V.'s FDA Establishment Identifier (FEI) is 3010263062.
Can shipments from Hul Kin, S.A. De C.V. still enter the U.S.?
Shipments of blue crab from Hul Kin, S.A. De C.V. 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.