Procesadora Uruapan, S. de R.L. de C.V.
FDA import alert and refusal historyTecate, MexicoFEI 3004790164
As of October 26, 2026, Procesadora Uruapan, S. de R.L. de C.V. (Tecate, Mexico) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for seafood salad (shrimp, crab, etc.), mixed fishery/seafood products, published by FDA on March 13, 2009, 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 16-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Procesadora Uruapan, S. de R.L. de C.V.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-39red listSeafood salad (shrimp, crab, etc.), Mixed Fishery/Seafood ProductsSource
Questions about Procesadora Uruapan, S. de R.L. de C.V.
- Is Procesadora Uruapan, S. de R.L. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Procesadora Uruapan, S. de R.L. de C.V. is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for seafood salad (shrimp, crab, etc.), mixed fishery/seafood products; FDA published the listing on March 13, 2009.
- Has FDA refused shipments from Procesadora Uruapan, S. de R.L. de C.V.?
- No FDA import refusals for Procesadora Uruapan, S. de R.L. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Procesadora Uruapan, S. de R.L. de C.V.'s FEI number?
- Procesadora Uruapan, S. de R.L. de C.V.'s FDA Establishment Identifier (FEI) is 3004790164.
- Can shipments from Procesadora Uruapan, S. de R.L. de C.V. still enter the U.S.?
- Shipments of seafood salad (shrimp, crab, etc.), mixed fishery/seafood products from Procesadora Uruapan, S. de R.L. de C.V. can be detained without physical examination under Import Alert 16-39; 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.