Filipi Company Shpk
FDA import alert and refusal historyLac, AlbaniaFEI 3010293006
As of October 26, 2026, Filipi Company Shpk (Lac, Albania) is on the red list of FDA Import Alert 99-42 (Foods: heavy metal (toxic element) contamination) for elderberry, published by FDA on August 4, 2023, is also listed on Import Alert 99-19 (red list), and has 13 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-42 · red listIA 99-19 · red list
- Last import refusal
- Herbals & botanicals (not teas), n.e.c. · POISONOUS
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Filipi Company Shpk
17 records, newest first. Each line links to the FDA page it came from.
2026
2025
- Import refusalRefused, Haw, dried or pasteFILTHYEntry W66-0143056-5Source
- Import refusalRefused, Herbals & botanical teas, n.e.c.POISONOUSEntry 8NW-1565531-4Source
- Import refusalRefused, Herbals & botanical teas, n.e.c.POISONOUSEntry 8NW-1566679-0Source
- Import refusalRefused, Sage, whole (spice)SALMONELLAEntry AQZ-0617666-6Source
- Import refusalRefused, Herbals & botanical teas, n.e.c.POISONOUSEntry 8NW-1565294-9Source
- Import refusalRefused, Elderberries (berry)POISONOUSEntry 8NW-1565293-1Source
2024
2023
- Import refusalRefused, Elderberries (berry)POISONOUSEntry ND7-2300386-6Source
- Import alert listingListed on Import Alert 99-42red listElderberrySource
2019
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2018
- Import refusalRefused, Sage, whole (spice)SALMONELLAEntry EYD-0917718-3Source
2017
Show 2 earlier records (2009–2017)Hide earlier records
2017
2009
- Import alert listingListed on Import Alert 99-19red listSage, Whole (Spice)Source
Refusal charges, in plain English
- POISONOUS8 refused lines
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
- FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- SALMONELLA2 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.
- MFR INSAN1 refused line
Insanitary manufacturing, processing or packing
The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.
Questions about Filipi Company Shpk
- Is Filipi Company Shpk on an FDA import alert?
- Yes. As of October 26, 2026, Filipi Company Shpk is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for elderberry; FDA published the listing on August 4, 2023.
- Has FDA refused shipments from Filipi Company Shpk?
- Yes. FDA refused 13 shipment lines from Filipi Company Shpk between July 6, 2017 and September 23, 2026. The most recent, on September 23, 2026, was herbals & botanicals (not teas), n.e.c., charged as POISONOUS (poisonous or deleterious substance).
- Why did FDA refuse Filipi Company Shpk's shipments?
- The most frequent charges are POISONOUS (poisonous or deleterious substance, 8 lines) and FILTHY (filthy, putrid or decomposed substance, 2 lines).
- When was Filipi Company Shpk last inspected by FDA?
- FDA's most recent inspection of Filipi Company Shpk with a final classification is dated August 27, 2024 and was classified NAI (No Action Indicated).
- What is Filipi Company Shpk's FEI number?
- Filipi Company Shpk's FDA Establishment Identifier (FEI) is 3010293006.
- Can shipments from Filipi Company Shpk still enter the U.S.?
- Shipments of elderberry from Filipi Company Shpk can be detained without physical examination under Import Alert 99-42; 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.