Empacond, S.A. de C.V.
FDA import alert and refusal historyMonterrey, MexicoFEI 3016885796
As of October 25, 2026, Empacond, S.A. de C.V. (Monterrey, Mexico) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for whole grain rice, published by FDA on September 16, 2009, 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 99-19 · red list
- Last import refusal
- Tamarind (subtropical/tropical fruit pulp) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Empacond, S.A. de C.V.
2 records, newest first. Each line links to the FDA page it came from.
2025
2009
- Import alert listingListed on Import Alert 99-19red listwhole grain riceSource
Refusal charges, in plain English
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Empacond, S.A. de C.V.
- Is Empacond, S.A. de C.V. on an FDA import alert?
- Yes. As of October 25, 2026, Empacond, S.A. de C.V. is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for whole grain rice; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Empacond, S.A. de C.V.?
- Yes. FDA refused 1 shipment line from Empacond, S.A. de C.V. on November 21, 2025. The most recent, on November 21, 2025, was tamarind (subtropical/tropical fruit pulp), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Empacond, S.A. de C.V.'s shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- What is Empacond, S.A. de C.V.'s FEI number?
- Empacond, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3016885796.
- Can shipments from Empacond, S.A. de C.V. still enter the U.S.?
- Shipments of whole grain rice from Empacond, S.A. de C.V. can be detained without physical examination under Import Alert 99-19; 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.