Gjedra
FDA import alert and refusal historyBerat, AlbaniaFEI 3011193134
As of October 26, 2026, Gjedra (Berat, Albania) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for whole dried sage, published by FDA on December 17, 2018, and has 3 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-19 · red list
- Last import refusal
- Sage, whole (spice) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Gjedra
5 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Sage, whole (spice)SALMONELLAEntry NMB-0001514-4Source
2025
- Import refusalRefused, Sage, whole (spice)SALMONELLAEntry AQZ-0615280-8Source
2023
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2019
- Import refusalRefused, Sage, whole (spice)SALMONELLAEntry CFV-0004266-2Source
2018
- Import alert listingListed on Import Alert 99-19red listWhole dried sageSource
Refusal charges, in plain English
- SALMONELLA3 refused lines
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Gjedra
- Is Gjedra on an FDA import alert?
- Yes. As of October 26, 2026, Gjedra is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for whole dried sage; FDA published the listing on December 17, 2018.
- Has FDA refused shipments from Gjedra?
- Yes. FDA refused 3 shipment lines from Gjedra between July 25, 2019 and August 16, 2026. The most recent, on August 16, 2026, was sage, whole (spice), charged as SALMONELLA (salmonella).
- Why did FDA refuse Gjedra's shipments?
- The most frequent charge is SALMONELLA (salmonella, 3 lines).
- When was Gjedra last inspected by FDA?
- FDA's most recent inspection of Gjedra with a final classification is dated January 17, 2023 and was classified VAI (Voluntary Action Indicated).
- What is Gjedra's FEI number?
- Gjedra's FDA Establishment Identifier (FEI) is 3011193134.
- Can shipments from Gjedra still enter the U.S.?
- Shipments of whole dried sage from Gjedra can be detained without physical examination under Import Alert 99-19; 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.