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El Zapotanito

FDA import alert and refusal historyLa Huerta, MexicoFEI 3010274476

Recorded by FDA as EL ZAPOTANITO

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

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As of October 26, 2026, El Zapotanito (La Huerta, Mexico) is on the red list of FDA Import Alert 99-35 (Fresh produce: insanitary conditions) for papayas, published by FDA on October 4, 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
Papaya (papaw) (subtropical and tropical fruit) · SALMONELLA
Last warning letter
None found
Last inspection
None on record

Every FDA record for El Zapotanito

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

2017

  1. Import alert listing
    Listed on Import Alert 99-35red listPapayas
    Source
  2. Import refusal
    Refused, Papaya (papaw) (subtropical and tropical fruit)SALMONELLAEntry DV1-0187164-3
    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 El Zapotanito

Is El Zapotanito on an FDA import alert?
Yes. As of October 26, 2026, El Zapotanito is on the red list of FDA Import Alert 99-35, “Fresh produce: insanitary conditions”, for papayas; FDA published the listing on October 4, 2017.
Has FDA refused shipments from El Zapotanito?
Yes. FDA refused 1 shipment line from El Zapotanito on August 17, 2017. The most recent, on August 17, 2017, was papaya (papaw) (subtropical and tropical fruit), charged as SALMONELLA (salmonella).
Why did FDA refuse El Zapotanito's shipments?
The most frequent charge is SALMONELLA (salmonella, 1 line).
What is El Zapotanito's FEI number?
El Zapotanito's FDA Establishment Identifier (FEI) is 3010274476.
Can shipments from El Zapotanito still enter the U.S.?
Shipments of papayas from El Zapotanito can be detained without physical examination under Import Alert 99-35; 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.