Corex
FDA import alert and refusal historyBattipaglia, ItalyFEI 3008260006
Recorded by FDA as COREX
As of October 25, 2026, Corex (Battipaglia, Italy) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for tri colored fusilli springs, published by FDA on February 2, 2017, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- Macaroni and spaghetti products,n.e.c. · STD IDENT
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Corex
2 records, newest first. Each line links to the FDA page it came from.
2020
2017
- Import alert listingListed on Import Alert 99-39red listTri Colored Fusilli SpringsSource
Refusal charges, in plain English
- STD IDENT1 refused line
Does not conform to standard of identity
The product appeared to be represented as a food that has an FDA standard of identity, but not to conform to that standard.
Questions about Corex
- Is Corex on an FDA import alert?
- Yes. As of October 25, 2026, Corex is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for tri colored fusilli springs; FDA published the listing on February 2, 2017.
- Has FDA refused shipments from Corex?
- Yes. FDA refused 1 shipment line from Corex on March 23, 2020. The most recent, on March 23, 2020, was macaroni and spaghetti products,n.e.c., charged as STD IDENT (does not conform to standard of identity).
- Why did FDA refuse Corex's shipments?
- The most frequent charge is STD IDENT (does not conform to standard of identity, 1 line).
- What is Corex's FEI number?
- Corex's FDA Establishment Identifier (FEI) is 3008260006.
- Can shipments from Corex still enter the U.S.?
- Shipments of tri colored fusilli springs from Corex can be detained without physical examination under Import Alert 99-39; 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.