Upi Productores, S. de R.L. de C.V.
FDA import alert and refusal historyFracc. San Quintin, MexicoFEI 2000015066
Recorded by FDA as UPI PRODUCTORES, S. DE R.L. DE C.V.
As of October 27, 2026, Upi Productores, S. de R.L. de C.V. (Fracc. San Quintin, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for brussels sprouts, published by FDA on April 28, 2014, and has no 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
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Upi Productores, S. de R.L. de C.V.
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-05red listBrussels SproutsSource
Questions about Upi Productores, S. de R.L. de C.V.
- Is Upi Productores, S. de R.L. de C.V. on an FDA import alert?
- Yes. As of October 27, 2026, Upi Productores, S. de R.L. de C.V. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for brussels sprouts; FDA published the listing on April 28, 2014.
- Has FDA refused shipments from Upi Productores, S. de R.L. de C.V.?
- No FDA import refusals for Upi Productores, S. de R.L. de C.V. appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Upi Productores, S. de R.L. de C.V.'s FEI number?
- Upi Productores, S. de R.L. de C.V.'s FDA Establishment Identifier (FEI) is 2000015066.
- Can shipments from Upi Productores, S. de R.L. de C.V. still enter the U.S.?
- Shipments of brussels sprouts from Upi Productores, S. de R.L. de C.V. 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.