HJR International Corporation
FDA import alert and refusal historyCebu, PhilippinesFEI 3004268798
As of October 26, 2026, HJR International Corporation (Cebu, Philippines) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for scallops; cuttlefish, other aquatic species, raw, fresh, ambient; cuttlefish, other aquatic species, raw, fresh, refrigerated; cuttlefish, other aquatic species, raw - fresh, frozen, natural state; scallops, aquaculture harvested fishery/seafood products, published by FDA on September 18, 2009, and has 7 FDA import refusals 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
- Shrimp & prawns · SALMONELLA
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for HJR International Corporation
9 records, newest first. Each line links to the FDA page it came from.
2020
- Import refusalRefused, Shrimp & prawnsSALMONELLAEntry 555-0679595-8Source
2019
- Import refusalRefused, Shrimp and prawns, aquaculture harvested fishery/seafood productsSALMONELLAEntry 991-0247011-1Source
- Import refusalRefused, Shrimp & prawnsSALMONELLAEntry 555-0673661-4Source
- Import refusalRefused, Shrimp & prawnsSALMONELLAEntry 555-0674645-6Source
- Import refusalSource
Refused, 3 lines in one entry: Shrimp & prawnsSALMONELLAEntry 555-0669855-8Show 3 linesHide lines
- Refused, Shrimp & prawnsSALMONELLAEntry 555-0669855-8Source
- Refused, Shrimp & prawnsSALMONELLAEntry 555-0669855-8Source
- Refused, Shrimp & prawnsSALMONELLAEntry 555-0669855-8Source
2015
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 16-81red listScallops; Cuttlefish, Other Aquatic Species, Raw, Fresh, Ambient; Cuttlefish, Other Aquatic Species, Raw, Fresh, Refrigerated; Cuttlefish, Other Aquatic Species, Raw - Fresh, Frozen, Natural State; Scallops, Aquaculture Harvested Fishery/Seafood ProductsSource
Refusal charges, in plain English
- SALMONELLA7 refused lines
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 HJR International Corporation
- Is HJR International Corporation on an FDA import alert?
- Yes. As of October 26, 2026, HJR International Corporation is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for scallops; cuttlefish, other aquatic species, raw, fresh, ambient; cuttlefish, other aquatic species, raw, fresh, refrigerated; cuttlefish, other aquatic species, raw - fresh, frozen, natural state; scallops, aquaculture harvested fishery/seafood products; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from HJR International Corporation?
- Yes. FDA refused 7 shipment lines from HJR International Corporation between April 16, 2019 and April 23, 2020. The most recent, on April 23, 2020, was shrimp & prawns, charged as SALMONELLA (salmonella).
- Why did FDA refuse HJR International Corporation's shipments?
- The most frequent charge is SALMONELLA (salmonella, 7 lines).
- When was HJR International Corporation last inspected by FDA?
- FDA's most recent inspection of HJR International Corporation with a final classification is dated September 24, 2015 and was classified VAI (Voluntary Action Indicated).
- What is HJR International Corporation's FEI number?
- HJR International Corporation's FDA Establishment Identifier (FEI) is 3004268798.
- Can shipments from HJR International Corporation still enter the U.S.?
- Shipments of scallops; cuttlefish, other aquatic species, raw, fresh, ambient; cuttlefish, other aquatic species, raw, fresh, refrigerated; cuttlefish, other aquatic species, raw - fresh, frozen, natural state; scallops, aquaculture harvested fishery/seafood products from HJR International Corporation 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.