Deshidratadora La Cascada S.A. De C.V.
FDA import alert and refusal historyVilla Corregidora Qu, MexicoFEI 1000271513
As of October 26, 2026, Deshidratadora La Cascada S.A. De C.V. (Villa Corregidora Qu, Mexico) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for dehydrated kale, published by FDA on September 16, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Deshidratadora La Cascada S.A. De C.V.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listdehydrated kaleSource
Questions about Deshidratadora La Cascada S.A. De C.V.
- Is Deshidratadora La Cascada S.A. De C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Deshidratadora La Cascada S.A. De C.V. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for dehydrated kale; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Deshidratadora La Cascada S.A. De C.V.?
- No FDA import refusals for Deshidratadora La Cascada S.A. De C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Deshidratadora La Cascada S.A. De C.V.'s FEI number?
- Deshidratadora La Cascada S.A. De C.V.'s FDA Establishment Identifier (FEI) is 1000271513.
- Can shipments from Deshidratadora La Cascada S.A. De C.V. still enter the U.S.?
- Shipments of dehydrated kale from Deshidratadora La Cascada 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.