A & C Fresh Produce
FDA import alert and refusal historyCocula, MexicoFEI 3013555166
Recorded by FDA as A & C FRESH PRODUCE
As of October 26, 2026, A & C Fresh Produce (Cocula, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for green beans, published by FDA on January 24, 2018, 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
- Stringbeans · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for A & C Fresh Produce
2 records, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 99-05red listGreen BeansSource
2017
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 A & C Fresh Produce
- Is A & C Fresh Produce on an FDA import alert?
- Yes. As of October 26, 2026, A & C Fresh Produce is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for green beans; FDA published the listing on January 24, 2018.
- Has FDA refused shipments from A & C Fresh Produce?
- Yes. FDA refused 1 shipment line from A & C Fresh Produce on December 15, 2017. The most recent, on December 15, 2017, was stringbeans, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse A & C Fresh Produce's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is A & C Fresh Produce's FEI number?
- A & C Fresh Produce's FDA Establishment Identifier (FEI) is 3013555166.
- Can shipments from A & C Fresh Produce still enter the U.S.?
- Shipments of green beans from A & C Fresh Produce 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.