Maspesca, SA de CV
FDA import alert and refusal historyProgreso, MexicoFEI 3004699126
As of October 26, 2026, Maspesca, SA de CV (Progreso, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for octopus, published by FDA on January 28, 2013, 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 16-81 · red list
- Last import refusal
- Octopus, other aquatic species · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Maspesca, SA de CV
2 records, newest first. Each line links to the FDA page it came from.
2023
- Import refusalRefused, Octopus, other aquatic speciesSALMONELLAEntry N55-0190334-2Source
2013
- Import alert listingListed on Import Alert 16-81red listOctopusSource
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 Maspesca, SA de CV
- Is Maspesca, SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Maspesca, SA de CV is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for octopus; FDA published the listing on January 28, 2013.
- Has FDA refused shipments from Maspesca, SA de CV?
- Yes. FDA refused 1 shipment line from Maspesca, SA de CV on July 14, 2023. The most recent, on July 14, 2023, was octopus, other aquatic species, charged as SALMONELLA (salmonella).
- Why did FDA refuse Maspesca, SA de CV's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Maspesca, SA de CV's FEI number?
- Maspesca, SA de CV's FDA Establishment Identifier (FEI) is 3004699126.
- Can shipments from Maspesca, SA de CV still enter the U.S.?
- Shipments of octopus from Maspesca, SA de CV can be detained without physical examination under Import Alert 16-81; 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.