SI O SI Alimentos
FDA import alert and refusal historyMorelia, MexicoFEI 3009800971
As of October 26, 2026, SI O SI Alimentos (Morelia, Mexico) is on the red list of FDA Import Alert 21-12 (Frozen and refrigerated guacamole and avocado products) for freeze dried avocado pulp powder, published by FDA on June 12, 2015, 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 21-12 · red list
- Last import refusal
- Avocado, dried or paste · LISTERIA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for SI O SI Alimentos
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- LISTERIA2 refused lines
Listeria monocytogenes
The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about SI O SI Alimentos
- Is SI O SI Alimentos on an FDA import alert?
- Yes. As of October 26, 2026, SI O SI Alimentos is on the red list of FDA Import Alert 21-12, “Frozen and refrigerated guacamole and avocado products”, for freeze dried avocado pulp powder; FDA published the listing on June 12, 2015.
- Has FDA refused shipments from SI O SI Alimentos?
- Yes. FDA refused 2 shipment lines from SI O SI Alimentos between November 2, 2018 and May 6, 2019. The most recent, on May 6, 2019, was avocado, dried or paste, charged as LISTERIA (listeria monocytogenes).
- Why did FDA refuse SI O SI Alimentos's shipments?
- The most frequent charge is LISTERIA (listeria monocytogenes, 2 lines).
- What is SI O SI Alimentos's FEI number?
- SI O SI Alimentos's FDA Establishment Identifier (FEI) is 3009800971.
- Can shipments from SI O SI Alimentos still enter the U.S.?
- Shipments of freeze dried avocado pulp powder from SI O SI Alimentos can be detained without physical examination under Import Alert 21-12; 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.