Agr.E.S. SRL
FDA import alert and refusal historyCarini, ItalyFEI 3004986896
Recorded by FDA as AGR.E.S. SRL
As of October 26, 2026, Agr.E.S. SRL (Carini, Italy) is on the red list of FDA Import Alert 99-47 (Foods that appear adulterated for economic gain) for sicilia lemon squeeze lemon juice, published by FDA on September 3, 2024, 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 99-47 · red list
- Last import refusal
- Lemon, citrus fruit juices or concentrates · ADDED BULK
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Agr.E.S. SRL
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalRefused, Lemon, citrus fruit juices or concentratesADDED BULKEntry 241-0318621-0Source
- Import alert listingListed on Import Alert 99-47red listSicilia Lemon Squeeze Lemon JuiceSource
Refusal charges, in plain English
- ADDED BULK1 refused line
ADDED BULK
Questions about Agr.E.S. SRL
- Is Agr.E.S. SRL on an FDA import alert?
- Yes. As of October 26, 2026, Agr.E.S. SRL is on the red list of FDA Import Alert 99-47, “Foods that appear adulterated for economic gain”, for sicilia lemon squeeze lemon juice; FDA published the listing on September 3, 2024.
- Has FDA refused shipments from Agr.E.S. SRL?
- Yes. FDA refused 1 shipment line from Agr.E.S. SRL on October 11, 2024. The most recent, on October 11, 2024, was lemon, citrus fruit juices or concentrates, charged as ADDED BULK (added bulk).
- Why did FDA refuse Agr.E.S. SRL's shipments?
- The most frequent charge is ADDED BULK (added bulk, 1 line).
- What is Agr.E.S. SRL's FEI number?
- Agr.E.S. SRL's FDA Establishment Identifier (FEI) is 3004986896.
- Can shipments from Agr.E.S. SRL still enter the U.S.?
- Shipments of sicilia lemon squeeze lemon juice from Agr.E.S. SRL can be detained without physical examination under Import Alert 99-47; 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.