Industrial Ganadera De Caborca
FDA import alert and refusal historyCaborca, MexicoFEI 3002762155
As of October 26, 2026, Industrial Ganadera De Caborca (Caborca, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for cucumbers, published by FDA on December 10, 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 99-23 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Industrial Ganadera De Caborca
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-23red listCucumbersSource
Questions about Industrial Ganadera De Caborca
- Is Industrial Ganadera De Caborca on an FDA import alert?
- Yes. As of October 26, 2026, Industrial Ganadera De Caborca is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for cucumbers; FDA published the listing on December 10, 2009.
- Has FDA refused shipments from Industrial Ganadera De Caborca?
- No FDA import refusals for Industrial Ganadera De Caborca appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Industrial Ganadera De Caborca's FEI number?
- Industrial Ganadera De Caborca's FDA Establishment Identifier (FEI) is 3002762155.
- Can shipments from Industrial Ganadera De Caborca still enter the U.S.?
- Shipments of cucumbers from Industrial Ganadera De Caborca can be detained without physical examination under Import Alert 99-23; 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).
Buying from Industrial Ganadera De Caborca?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.