Jesus Alberto Valdez Uriarte
FDA import alert and refusal historyEnsenada, MexicoFEI 3011255500
As of October 26, 2026, Jesus Alberto Valdez Uriarte (Ensenada, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for prickley pear cactus edible stems or pads/nopal; fresh cactus, published by FDA on March 18, 2015, 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 Jesus Alberto Valdez Uriarte
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-05red listPrickley Pear Cactus Edible Stems or Pads/Nopal; Fresh CactusSource
Questions about Jesus Alberto Valdez Uriarte
- Is Jesus Alberto Valdez Uriarte on an FDA import alert?
- Yes. As of October 26, 2026, Jesus Alberto Valdez Uriarte is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for prickley pear cactus edible stems or pads/nopal; fresh cactus; FDA published the listing on March 18, 2015.
- Has FDA refused shipments from Jesus Alberto Valdez Uriarte?
- No FDA import refusals for Jesus Alberto Valdez Uriarte appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Jesus Alberto Valdez Uriarte's FEI number?
- Jesus Alberto Valdez Uriarte's FDA Establishment Identifier (FEI) is 3011255500.
- Can shipments from Jesus Alberto Valdez Uriarte still enter the U.S.?
- Shipments of prickley pear cactus edible stems or pads/nopal; fresh cactus from Jesus Alberto Valdez Uriarte 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.