Hai Son Foods
FDA import alert and refusal historyNhatrang, VietnamFEI 3009944073
As of October 26, 2026, Hai Son Foods (Nhatrang, Vietnam) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tinfoil barb; grouper; mullet fish; fusilier; scad; mud fish; bream; trevally; bream & gold band fusilier; crab; shrimp, published by FDA on September 30, 2009, is also listed on Import Alert 16-125 (green list), and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-125 · green listIA 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hai Son Foods
2 records, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 16-125green listBarramundiSource
2009
- Import alert listingListed on Import Alert 16-81red listTinfoil Barb; Grouper; Mullet Fish; Fusilier; Scad; Mud Fish; Bream; Trevally; Bream & Gold Band Fusilier; Crab; ShrimpSource
Questions about Hai Son Foods
- Is Hai Son Foods on an FDA import alert?
- Yes. As of October 26, 2026, Hai Son Foods is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tinfoil barb; grouper; mullet fish; fusilier; scad; mud fish; bream; trevally; bream & gold band fusilier; crab; shrimp; FDA published the listing on September 30, 2009.
- Has FDA refused shipments from Hai Son Foods?
- No FDA import refusals for Hai Son Foods appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Hai Son Foods's FEI number?
- Hai Son Foods's FDA Establishment Identifier (FEI) is 3009944073.
- Can shipments from Hai Son Foods still enter the U.S.?
- Shipments of tinfoil barb; grouper; mullet fish; fusilier; scad; mud fish; bream; trevally; bream & gold band fusilier; crab; shrimp from Hai Son Foods 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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