Maya Vegetables Inc
FDA import alert and refusal historyEnenada, MexicoFEI 3010205368
As of October 26, 2026, Maya Vegetables Inc (Enenada, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for mexican squash, published by FDA on October 3, 2023, and has 2 FDA import refusals 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 Maya Vegetables Inc
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 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.
Questions about Maya Vegetables Inc
- Is Maya Vegetables Inc on an FDA import alert?
- Yes. As of October 26, 2026, Maya Vegetables Inc is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for mexican squash; FDA published the listing on October 3, 2023.
- Has FDA refused shipments from Maya Vegetables Inc?
- Yes. FDA refused 2 shipment lines from Maya Vegetables Inc between September 28, 2023 and May 13, 2026. The most recent, on May 13, 2026, was squash, summer (fruit used as vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Maya Vegetables Inc's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Maya Vegetables Inc's FEI number?
- Maya Vegetables Inc's FDA Establishment Identifier (FEI) is 3010205368.
- Can shipments from Maya Vegetables Inc still enter the U.S.?
- Shipments of mexican squash from Maya Vegetables Inc 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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