Xsant, S.A. de C.V.
FDA import alert and refusal historyPueblo Rayon, MexicoFEI 3013821887
As of October 26, 2026, Xsant, S.A. de C.V. (Pueblo Rayon, Mexico) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for cactus in brine, published by FDA on March 14, 2019, 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 99-08 · red list
- Last import refusal
- Leaf & stem vegetables, n.e.c. · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Xsant, S.A. de C.V.
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 Xsant, S.A. de C.V.
- Is Xsant, S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Xsant, S.A. de C.V. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for cactus in brine; FDA published the listing on March 14, 2019.
- Has FDA refused shipments from Xsant, S.A. de C.V.?
- Yes. FDA refused 2 shipment lines from Xsant, S.A. de C.V. between March 13, 2019 and April 24, 2019. The most recent, on April 24, 2019, was leaf & stem vegetables, n.e.c., charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Xsant, S.A. de C.V.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Xsant, S.A. de C.V.'s FEI number?
- Xsant, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3013821887.
- Can shipments from Xsant, S.A. de C.V. still enter the U.S.?
- Shipments of cactus in brine from Xsant, S.A. de C.V. can be detained without physical examination under Import Alert 99-08; 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.