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Cilanmex de San Juan S.P.R de R.L.

FDA import alert and refusal historyLos Reyes De Juarez, MexicoFEI 3009841812

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Example subjectCilanmex de San Juan S.P.R de R.L added to Import Alert 16-129 (red list)

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As of October 26, 2026, Cilanmex de San Juan S.P.R de R.L. (Los Reyes De Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for celery; coriander (cilantro), published by FDA on April 24, 2017, and has 10 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Cilantro (leaf & stem vegetable) · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Cilanmex de San Juan S.P.R de R.L.

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

2020

  1. Import refusal
    Refused, Cilantro (leaf & stem vegetable)PESTICIDEEntry BYX-0171173-2
    Source

2019

  1. Import refusal
    Refused, Cilantro (leaf & stem vegetable)PESTICIDEEntry BYX-0157603-6
    Source

2018

  1. Import refusal
    Refused, Cilantro (leaf & stem vegetable)PESTICIDEEntry BJG-0063268-6
    Source
  2. Import refusal
    Refused, Cilantro (leaf & stem vegetable)PESTICIDEINSANITARYMFR INSANEntry BJG-0061408-0
    Source
  3. Import refusal
    Refused, Celery (leaf & stem vegetable)PESTICIDEEntry BJG-0059753-3
    Source
  4. Import refusal
    Refused, Celery (leaf & stem vegetable)PESTICIDEEntry BJG-0060424-8
    Source
  5. Import refusal
    Refused, Celery (leaf & stem vegetable)PESTICIDEEntry BJG-0060036-0
    Source
  6. Import refusal
    Refused, Celery (leaf & stem vegetable)PESTICIDEEntry BJG-0060199-6
    Source

2017

  1. Import refusal
    Refused, Celery (leaf & stem vegetable)PESTICIDEEntry BJG-0048981-4
    Source
  2. Import refusal
    Refused, Cilantro (leaf & stem vegetable)PESTICIDEEntry B9A-0001360-5
    Source
  3. Import alert listing
    Listed on Import Alert 99-05red listCelery; Coriander (Cilantro)
    Source

Refusal charges, in plain English

  • PESTICIDE10 refused lines

    Pesticide chemical residue

    The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

  • INSANITARY1 refused line

    Prepared, packed or held under insanitary conditions

    The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth or rendered injurious to health.

  • MFR INSAN1 refused line

    Insanitary manufacturing, processing or packing

    The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

Questions about Cilanmex de San Juan S.P.R de R.L.

Is Cilanmex de San Juan S.P.R de R.L. on an FDA import alert?
Yes. As of October 26, 2026, Cilanmex de San Juan S.P.R de R.L. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for celery; coriander (cilantro); FDA published the listing on April 24, 2017.
Has FDA refused shipments from Cilanmex de San Juan S.P.R de R.L.?
Yes. FDA refused 10 shipment lines from Cilanmex de San Juan S.P.R de R.L. between April 26, 2017 and January 30, 2020. The most recent, on January 30, 2020, was cilantro (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Cilanmex de San Juan S.P.R de R.L.'s shipments?
The most frequent charges are PESTICIDE (pesticide chemical residue, 10 lines) and INSANITARY (prepared, packed or held under insanitary conditions, 1 line).
What is Cilanmex de San Juan S.P.R de R.L.'s FEI number?
Cilanmex de San Juan S.P.R de R.L.'s FDA Establishment Identifier (FEI) is 3009841812.
Can shipments from Cilanmex de San Juan S.P.R de R.L. still enter the U.S.?
Shipments of celery; coriander (cilantro) from Cilanmex de San Juan S.P.R de R.L. can be detained without physical examination under Import Alert 99-05; 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.