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INVERNADEROS SAN EDUARDO S. de P.R. de R.L.

FDA import alert and refusal historyVilla Juarez, MexicoFEI 3010146191

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Example subjectINVERNADEROS SAN EDUARDO S. de P.R. de R.L added to Import Alert 16-129 (red list)

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As of October 27, 2026, INVERNADEROS SAN EDUARDO S. de P.R. de R.L. (Villa Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for sweet bell peppers, published by FDA on October 29, 2015, and has 7 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Cucumbers (fruit used as vegetable) · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for INVERNADEROS SAN EDUARDO S. de P.R. de R.L.

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

2022

  1. Import refusal
    Refused, Cucumbers (fruit used as vegetable)PESTICIDELACKS FIRMLACKS N/CEntry M92-5096843-2
    Source

2017

  1. Import refusal
    Refused, Pepper, sweet (fruit used as vegetable)PESTICIDEEntry M92-5066285-2
    Source
  2. Import refusal
    Refused, 5 lines in one entry: Pepper, sweet (fruit used as vegetable)PESTICIDEEntry M92-5066232-4Show 5 lines
    • Refused, Pepper, sweet (fruit used as vegetable)PESTICIDEEntry M92-5066232-4Source
    • Refused, Pepper, sweet (fruit used as vegetable)PESTICIDEEntry M92-5066232-4Source
    • Refused, Pepper, sweet (fruit used as vegetable)PESTICIDEEntry M92-5066232-4Source
    • Refused, Pepper, sweet (fruit used as vegetable)PESTICIDEEntry M92-5066232-4Source
    • Refused, Pepper, sweet (fruit used as vegetable)PESTICIDEEntry M92-5066232-4Source
    Source

2015

  1. Import alert listing
    Listed on Import Alert 99-05red listSweet Bell Peppers
    Source

Refusal charges, in plain English

  • PESTICIDE7 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.

  • LACKS FIRM1 refused line

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

Questions about INVERNADEROS SAN EDUARDO S. de P.R. de R.L.

Is INVERNADEROS SAN EDUARDO S. de P.R. de R.L. on an FDA import alert?
Yes. As of October 27, 2026, INVERNADEROS SAN EDUARDO S. de P.R. de R.L. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for sweet bell peppers; FDA published the listing on October 29, 2015.
Has FDA refused shipments from INVERNADEROS SAN EDUARDO S. de P.R. de R.L.?
Yes. FDA refused 7 shipment lines from INVERNADEROS SAN EDUARDO S. de P.R. de R.L. between June 9, 2017 and May 16, 2022. The most recent, on May 16, 2022, was cucumbers (fruit used as vegetable), charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse INVERNADEROS SAN EDUARDO S. de P.R. de R.L.'s shipments?
The most frequent charges are PESTICIDE (pesticide chemical residue, 7 lines) and LACKS FIRM (manufacturer name and address missing, 1 line).
What is INVERNADEROS SAN EDUARDO S. de P.R. de R.L.'s FEI number?
INVERNADEROS SAN EDUARDO S. de P.R. de R.L.'s FDA Establishment Identifier (FEI) is 3010146191.
Can shipments from INVERNADEROS SAN EDUARDO S. de P.R. de R.L. still enter the U.S.?
Shipments of sweet bell peppers from INVERNADEROS SAN EDUARDO S. de 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.