Mariscos de Corazon Mc S.A.
FDA import alert and refusal historyPuntarenas, Costa RicaFEI 3013773125
Recorded by FDA as MARISCOS DE CORAZON MC S.A.
As of October 26, 2026, Mariscos de Corazon Mc S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 28, 2024, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Sturgeon (river and sea), hot smoked, fish · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Mariscos de Corazon Mc S.A.
1 record, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Mariscos de Corazon Mc S.A.
- Is Mariscos de Corazon Mc S.A. on an FDA import alert?
- No listing for Mariscos de Corazon Mc S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Costa Rica page.
- Has FDA refused shipments from Mariscos de Corazon Mc S.A.?
- Yes. FDA refused 1 shipment line from Mariscos de Corazon Mc S.A. on February 28, 2024. The most recent, on February 28, 2024, was sturgeon (river and sea), hot smoked, fish, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Mariscos de Corazon Mc S.A.'s shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- What is Mariscos de Corazon Mc S.A.'s FEI number?
- Mariscos de Corazon Mc S.A.'s FDA Establishment Identifier (FEI) is 3013773125.
Buying from Mariscos de Corazon Mc S.A.?
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.