EPO S.r.l.
FDA import alert and refusal historyMilan, ItalyFEI 3011282591
As of October 26, 2026, EPO S.r.l. (Milan, Italy) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for bilberry extract, published by FDA on July 16, 2013, 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 99-08 · red list
- Last import refusal
- Bilberry (herbal & botanicals, not teas) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for EPO S.r.l.
2 records, newest first. Each line links to the FDA page it came from.
2020
2013
- Import alert listingListed on Import Alert 99-08red listBilberry ExtractSource
Refusal charges, in plain English
- PESTICIDE1 refused line
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about EPO S.r.l.
- Is EPO S.r.l. on an FDA import alert?
- Yes. As of October 26, 2026, EPO S.r.l. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for bilberry extract; FDA published the listing on July 16, 2013.
- Has FDA refused shipments from EPO S.r.l.?
- Yes. FDA refused 1 shipment line from EPO S.r.l. on April 23, 2020. The most recent, on April 23, 2020, was bilberry (herbal & botanicals, not teas), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse EPO S.r.l.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is EPO S.r.l.'s FEI number?
- EPO S.r.l.'s FDA Establishment Identifier (FEI) is 3011282591.
- Can shipments from EPO S.r.l. still enter the U.S.?
- Shipments of bilberry extract from EPO S.r.l. can be detained without physical examination under Import Alert 99-08; 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.