Gerardo Maciel
FDA import alert and refusal historyEnsenada, MexicoFEI 3027024903
Recorded by FDA as GERARDO MACIEL
As of October 25, 2026, Gerardo Maciel (Ensenada, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for mexican squash, published by FDA on October 16, 2014, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- Squash, summer (fruit used as vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Gerardo Maciel
2 records, newest first. Each line links to the FDA page it came from.
2024
2014
- Import alert listingListed on Import Alert 99-05red listMexican SquashSource
Refusal charges, in plain English
- PESTICIDE1 refused line
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.
Questions about Gerardo Maciel
- Is Gerardo Maciel on an FDA import alert?
- Yes. As of October 25, 2026, Gerardo Maciel is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for mexican squash; FDA published the listing on October 16, 2014.
- Has FDA refused shipments from Gerardo Maciel?
- Yes. FDA refused 1 shipment line from Gerardo Maciel on May 3, 2024. The most recent, on May 3, 2024, was squash, summer (fruit used as vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Gerardo Maciel's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Gerardo Maciel's FEI number?
- Gerardo Maciel's FDA Establishment Identifier (FEI) is 3027024903.
- Can shipments from Gerardo Maciel still enter the U.S.?
- Shipments of mexican squash from Gerardo Maciel 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.