U.S. flag An official website of the United States government
  1. Home
  2. Inspections, Compliance, Enforcement, and Criminal Investigations
  3. Compliance Actions and Activities
  4. Warning Letters
  5. Promar Seafood S. de R.L. - 625993 - 03/01/2023
  1. Warning Letters


Promar Seafood S. de R.L. MARCS-CMS 625993 —

Delivery Method:
Via Express Delivery
Food & Beverages

Recipient Name
Mr. Riley Gough
Recipient Title
Promar Seafood S. de R.L.

Contiguo A La Naval
Carretera Muelle De Cabotaje
La Ceiba,

Issuing Office:
Center for Food Safety and Applied Nutrition (CFSAN)

United States

March 1, 2022


Reference # 625993

Dear Riley Gough:

The United States Food and Drug Administration (FDA) conducted a Foreign Remote Regulatory Assessment (FRRA) of your seafood processing facility, located at Promar Seafood S. de R.L. located at Contiguo A La Naval, Carretera Muelle De Cabotaje, La Ceiba, Atlantida, Honduras, on January 5 through 12, 2022. An on-site inspection was not possible due to travel restrictions during the COVID-19 pandemic. During the remote assessment, we found that you had serious violations of the seafood Hazard Analysis and Critical Control Point (HACCP) regulation, Title 21, Code of Federal Regulations (21 CFR Part 123). At the conclusion of the assessment, the FDA investigator discussed items of concern. To date, your firm has not responded to the discussion items identified during the FFRA.

In accordance with 21 CFR 123.6(g), failure of a processor of fish or fishery products to have and implement a HACCP plan that complies with this section or otherwise operate in accordance with the requirements of Part 123, renders the fish or fishery products adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug and Cosmetic Act (the Act), 21 U.S.C. § 342(a)(4). Accordingly, your cooked, dried, shelf-stable, sea cucumber products are adulterated, in that they have been prepared, packed, or held under conditions whereby they may have been rendered injurious to health. You may find the Act, the seafood HACCP regulation and the 4th Edition of the Fish and Fisheries Products Hazards and Controls Guidance (the Hazards Guide) through links in FDA's home page at www.fda.gov.

Your significant deviation is as follows:

• You do not have a written HACCP plan that outlines controls for a food safety hazard that is reasonably likely to occur as required by 21 CFR 123.6(b). Specifically, you do not have a HACCP plan for your cooked, dried, shelf-stable, sea cucumber products intended for the U.S. market to control the hazard of pathogenic bacteria growth and toxin formation including Staphylococcus aureus.

Your hazard analysis and flow chart indicate a (b)(4) step with multiple (b)(4) steps and then a (b)(4) step that is critical safety barrier for products distributed without refrigeration. The hazard analysis identifies pathogen hazards, but considers the hazards prevented or controlled through the implementation of pre-requisite programs.

You should respond in writing within fifteen (15) working days from your receipt of this letter. Your response should outline the specific steps you are taking to correct these deviations. More specifically, your response should include documentation reflecting the changes you made, such as a copy of your revised HACCP plan or plans, five (5) consecutive days of completed monitoring records (i.e., complete sets of monitoring records for the production of 5 production date codes of products) to demonstrate implementation of the plan, and any additional information that you wish to supply that provides assurance of your intent to fully comply now and in the future with the seafood HACCP regulation. If you cannot complete all corrections within 15 days, you should explain the reason for your delay and state when you will correct any remaining violations. If you believe that your product is not in violation of the Act, include your reasoning and any supporting information for our consideration.

If you do not respond or if we find your response inadequate, we may take further action. For instance, we may take further action to refuse admission of your imported fish or fishery products under Section 801(a) of the Act (21 U.S.C. § 381(a)), including placing them on detention without physical examination (DWPE). FDA’s DWPE is an administrative procedure whereby products offered for import into the United States may be detained without physical examination upon entry. DWPE information may be conveyed in FDA’s Import Alerts. For your information, an example of an Import Alert that conveys information specific to foreign firms that are not in compliance with the seafood HACCP regulation is Import Alert #16-120. You may view this alert at: http://www.accessdata.fda.gov/cms_ia/ialist.html.

This letter may not list all the deviations at your facility. You are responsible for ensuring that your processing plant operates in compliance with the Act and all applicable regulations, including the seafood HACCP regulation and the Current Good Manufacturing Practice regulation (21 CFR Part 117, Subpart B). You also have a responsibility to use procedures to prevent further violations of the Act and all applicable regulations.

You should direct your written reply to Rosemary Sexton, Food and Drug Administration, Center for Food Safety and Applied Nutrition, 5001 Campus Drive, Office of Compliance (HFS-608), Division of Enforcement, College Park, Maryland 20740-3835. If you have any questions regarding this letter, you may contact Rosemary Sexton via email at Rosemary.Sexton@fda.hhs.gov. Please reference CMS #625993 on any submissions and on the subject line of any emails to us.


Ann M. Oxenham
Acting Director
Office of Compliance
Center for Food Safety and Applied Nutrition

Back to Top