Jose Juan Acosta Meza
FDA import alert and refusal historyLos Mochis, MexicoFEI 3012647799
Recorded by FDA as JOSE JUAN ACOSTA MEZA
As of October 27, 2026, Jose Juan Acosta Meza (Los Mochis, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for corn, published by FDA on December 23, 2019, 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 99-23 · red list
- Last import refusal
- Corn, (vegetable) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Jose Juan Acosta Meza
2 records, newest first. Each line links to the FDA page it came from.
2019
- Import alert listingListed on Import Alert 99-23red listCornSource
- Import refusalRefused, Corn, (vegetable)SALMONELLAEntry 9QW-1247758-2Source
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 Jose Juan Acosta Meza
- Is Jose Juan Acosta Meza on an FDA import alert?
- Yes. As of October 27, 2026, Jose Juan Acosta Meza is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for corn; FDA published the listing on December 23, 2019.
- Has FDA refused shipments from Jose Juan Acosta Meza?
- Yes. FDA refused 1 shipment line from Jose Juan Acosta Meza on December 10, 2019. The most recent, on December 10, 2019, was corn, (vegetable), charged as SALMONELLA (salmonella).
- Why did FDA refuse Jose Juan Acosta Meza's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Jose Juan Acosta Meza's FEI number?
- Jose Juan Acosta Meza's FDA Establishment Identifier (FEI) is 3012647799.
- Can shipments from Jose Juan Acosta Meza still enter the U.S.?
- Shipments of corn from Jose Juan Acosta Meza 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).
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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.