Roberto Antonio Acosta Guzman
FDA import alert and refusal historyLa Paz, MexicoFEI 3013482179
Recorded by FDA as ROBERTO ANTONIO ACOSTA GUZMAN
As of October 26, 2026, Roberto Antonio Acosta Guzman (La Paz, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for pasilla peppers, published by FDA on July 7, 2017, and has 2 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
- Pepper, hot, n.e.c. (fruit used as vegetable) · POISONOUS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Roberto Antonio Acosta Guzman
3 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalSource
Refused, 2 lines in one entry: Pepper, hot, n.e.c. (fruit used as vegetable)POISONOUSEntry BHK-6051379-2Show 2 linesHide lines
2017
- Import alert listingListed on Import Alert 99-23red listPasilla PeppersSource
Refusal charges, in plain English
- POISONOUS2 refused lines
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
Questions about Roberto Antonio Acosta Guzman
- Is Roberto Antonio Acosta Guzman on an FDA import alert?
- Yes. As of October 26, 2026, Roberto Antonio Acosta Guzman is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for pasilla peppers; FDA published the listing on July 7, 2017.
- Has FDA refused shipments from Roberto Antonio Acosta Guzman?
- Yes. FDA refused 2 shipment lines from Roberto Antonio Acosta Guzman on February 22, 2018. The most recent, on February 22, 2018, was pepper, hot, n.e.c. (fruit used as vegetable), charged as POISONOUS (poisonous or deleterious substance).
- Why did FDA refuse Roberto Antonio Acosta Guzman's shipments?
- The most frequent charge is POISONOUS (poisonous or deleterious substance, 2 lines).
- What is Roberto Antonio Acosta Guzman's FEI number?
- Roberto Antonio Acosta Guzman's FDA Establishment Identifier (FEI) is 3013482179.
- Can shipments from Roberto Antonio Acosta Guzman still enter the U.S.?
- Shipments of pasilla peppers from Roberto Antonio Acosta Guzman 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 Roberto Antonio Acosta Guzman?
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.