Tuta Corporation

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

Refusal charges, in plain English

• NITROFURAN1 refused line

  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.

• VETDRUGRES1 refused line

  Animal drug residue

  The product appeared to contain a new animal drug, or a conversion product of one, that is unsafe within the meaning of section 512 of the FD&C Act.

Questions about Tuta Corporation

Is Tuta Corporation on an FDA import alert?

Yes. As of October 26, 2026, Tuta Corporation is on the red list of FDA Import Alert 16-129, “Seafood products: nitrofurans”, for shrimp; FDA published the listing on October 18, 2017.

Has FDA refused shipments from Tuta Corporation?

Yes. FDA refused 2 shipment lines from Tuta Corporation between September 20, 2017 and October 22, 2019. The most recent, on October 22, 2019, was shrimp & prawns, charged as NITROFURAN (nitrofurans).

Why did FDA refuse Tuta Corporation's shipments?

The most frequent charges are NITROFURAN (nitrofurans, 1 line) and VETDRUGRES (animal drug residue, 1 line).

What is Tuta Corporation's FEI number?

Tuta Corporation's FDA Establishment Identifier (FEI) is 3009987515.

Can shipments from Tuta Corporation still enter the U.S.?

Shipments of shrimp from Tuta Corporation can be detained without physical examination under Import Alert 16-129; 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).