Fruteria Mendoza
FDA import alert and refusal historyJuarez, MexicoFEI 3010113449
Recorded by FDA as FRUTERIA MENDOZA
As of October 26, 2026, Fruteria Mendoza (Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh key limes; papaya; fresh pineapples; poblano pepper; jalapeno peppers; cucumber; tomatoes; cactus leaves; cactus leaves, published by FDA on January 14, 2010, 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 Fruteria Mendoza
1 record, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 99-05red listFresh Key Limes; Papaya; Fresh Pineapples; Poblano Pepper; Jalapeno Peppers; Cucumber; Tomatoes; Cactus leaves; Cactus LeavesSource
Questions about Fruteria Mendoza
- Is Fruteria Mendoza on an FDA import alert?
- Yes. As of October 26, 2026, Fruteria Mendoza is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh key limes; papaya; fresh pineapples; poblano pepper; jalapeno peppers; cucumber; tomatoes; cactus leaves; cactus leaves; FDA published the listing on January 14, 2010.
- Has FDA refused shipments from Fruteria Mendoza?
- No FDA import refusals for Fruteria Mendoza appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Fruteria Mendoza's FEI number?
- Fruteria Mendoza's FDA Establishment Identifier (FEI) is 3010113449.
- Can shipments from Fruteria Mendoza still enter the U.S.?
- Shipments of fresh key limes; papaya; fresh pineapples; poblano pepper; jalapeno peppers; cucumber; tomatoes; cactus leaves; cactus leaves from Fruteria Mendoza 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.