Hector Mauricio Tamayo Ibarra
FDA import alert and refusal historyCiudad De Armeria, MexicoFEI 3012696647
As of October 26, 2026, Hector Mauricio Tamayo Ibarra is on the green list of FDA Import Alert 21-17, which exempts its listed products from detention without physical examination under that alert, 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 21-17 · green list
- Last import refusal
- Papaya (papaw) (subtropical and tropical fruit) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hector Mauricio Tamayo Ibarra
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import alert listingListed on Import Alert 21-17green listPapayaSource
2016
- Import refusalRefused, Papaya (papaw) (subtropical and tropical fruit)SALMONELLAEntry BVG-0032371-7Source
Refusal charges, in plain English
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Hector Mauricio Tamayo Ibarra
- Is Hector Mauricio Tamayo Ibarra on an FDA import alert?
- Yes. As of October 26, 2026, Hector Mauricio Tamayo Ibarra is on the green list of FDA Import Alert 21-17, “Papaya from Mexico”, for papaya; FDA published the listing on July 7, 2017.
- Has FDA refused shipments from Hector Mauricio Tamayo Ibarra?
- Yes. FDA refused 1 shipment line from Hector Mauricio Tamayo Ibarra on October 31, 2016. The most recent, on October 31, 2016, was papaya (papaw) (subtropical and tropical fruit), charged as SALMONELLA (salmonella).
- Why did FDA refuse Hector Mauricio Tamayo Ibarra's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Hector Mauricio Tamayo Ibarra's FEI number?
- Hector Mauricio Tamayo Ibarra's FDA Establishment Identifier (FEI) is 3012696647.
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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.