Hortil SA
FDA import alert and refusal historyXeresa, SpainFEI 8972
As of October 25, 2026, Hortil SA (Xeresa, Spain) is on the red list of FDA Import Alert 99-37 (Low-acid canned/acidified foods without scheduled process) for mushrooms (whole) in brine; mushrooms (pieces and stems) in brine; mushrooms (sliced) in brine; mushrooms in brine, published by FDA on June 3, 2014, 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 99-37 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hortil SA
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-37red listMUSHROOMS (WHOLE) IN BRINE; MUSHROOMS (PIECES AND STEMS) IN BRINE; MUSHROOMS (SLICED) IN BRINE; Mushrooms in brineSource
Questions about Hortil SA
- Is Hortil SA on an FDA import alert?
- Yes. As of October 25, 2026, Hortil SA is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for mushrooms (whole) in brine; mushrooms (pieces and stems) in brine; mushrooms (sliced) in brine; mushrooms in brine; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Hortil SA?
- No FDA import refusals for Hortil SA appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Hortil SA's FEI number?
- Hortil SA's FDA Establishment Identifier (FEI) is 8972.
- Can shipments from Hortil SA still enter the U.S.?
- Shipments of mushrooms (whole) in brine; mushrooms (pieces and stems) in brine; mushrooms (sliced) in brine; mushrooms in brine from Hortil SA can be detained without physical examination under Import Alert 99-37; 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.