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Propemar S.A.

FDA import alert and refusal historyMontecristi, EcuadorFEI 2000033174

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Example subjectPropemar S.A added to Import Alert 16-129 (red list)

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As of October 25, 2026, Propemar S.A. is on the green list of FDA Import Alert 16-05, which exempts its listed products from detention without physical examination under that alert, and has 25 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
IA 16-05 · green list
Last import refusal
Shrimp and prawns, aquaculture harvested fishery/seafood products · NITROFURAN
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Propemar S.A.

28 records, newest first. Each line links to the FDA page it came from.

2024

  1. Import refusal
    Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry D97-1960361-2
    Source

2023

  1. Import refusal
    Refused, 2 lines in one entry: Mahi mahiFILTHYEntry 594-0364508-4Show 2 lines
    Source
  2. Import refusal
    Refused, 6 lines in one entry: Mahi mahiFILTHYEntry CDX-0083868-2Show 6 lines
    Source
  3. Import refusal
    Refused, Mahi mahiFILTHYEntry RD8-0023627-8
    Source
  4. Import refusal
    Refused, 3 lines in one entry: Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 594-0357126-4Show 3 lines
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 594-0357126-4Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 594-0357126-4Source
    • Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsNITROFURANEntry 594-0357126-4Source
    Source

2022

  1. Import refusal
    Refused, 2 lines in one entry: Mahi mahiFILTHYLACKS FIRMFILTHEntry 594-0352582-3Show 2 lines
    Source
  2. Import refusal
    Refused, 3 lines in one entry: Mahi mahiFILTHYLACKS FIRMEntry 594-0354012-9Show 3 lines
    Source

2018

  1. Import refusal
    Refused, 2 lines in one entry: SwordfishFILTHYEntry 594-0297511-0Show 2 lines
    Source

2017

  1. Import refusal
    Refused, 5 lines in one entry: SwordfishFILTHYEntry 594-0283785-6Show 5 lines
    Source
  2. Import alert listing
    Listed on Import Alert 16-05green listMahi Mahi
    Source

2016

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2013

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • FILTHY20 refused lines

    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.

  • LACKS FIRM5 refused lines

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • NITROFURAN4 refused lines

    Nitrofurans

    The product appeared to contain nitrofurans, a class of antibiotic drugs, which are treated as an unsafe food additive under section 409 of the FD&C Act.

  • FILTH1 refused line

    FILTH

Questions about Propemar S.A.

Is Propemar S.A. on an FDA import alert?
Yes. As of October 25, 2026, Propemar S.A. is on the green list of FDA Import Alert 16-05, “Mahimahi from Ecuador and Taiwan: histamine, decomposition”, for mahi mahi; FDA published the listing on January 24, 2017.
Has FDA refused shipments from Propemar S.A.?
Yes. FDA refused 25 shipment lines from Propemar S.A. between September 11, 2017 and January 11, 2024. The most recent, on January 11, 2024, was shrimp and prawns, aquaculture harvested fishery/seafood products, charged as NITROFURAN (nitrofurans).
Why did FDA refuse Propemar S.A.'s shipments?
The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 20 lines) and LACKS FIRM (manufacturer name and address missing, 5 lines).
When was Propemar S.A. last inspected by FDA?
FDA's most recent inspection of Propemar S.A. with a final classification is dated November 14, 2016 and was classified NAI (No Action Indicated).
What is Propemar S.A.'s FEI number?
Propemar S.A.'s FDA Establishment Identifier (FEI) is 2000033174.

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Example subjectPropemar S.A added to Import Alert 16-129 (red list)

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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.