SC PlantExtrakt
FDA import alert and refusal historyRadaia, RomaniaFEI 3010698715
As of October 26, 2026, SC PlantExtrakt (Radaia, Romania) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for uti relief; silver birch; common fig; black currant; allergy relief; anxiety relief; digestive relief; earache relief; flu relief, published by FDA on March 23, 2017, 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 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for SC PlantExtrakt
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import alert listingListed on Import Alert 99-39red listUTI Relief; Silver Birch; Common Fig; Black Currant; Allergy Relief; Anxiety Relief; Digestive Relief; Earache Relief; Flu ReliefSource
Questions about SC PlantExtrakt
- Is SC PlantExtrakt on an FDA import alert?
- Yes. As of October 26, 2026, SC PlantExtrakt is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for uti relief; silver birch; common fig; black currant; allergy relief; anxiety relief; digestive relief; earache relief; flu relief; FDA published the listing on March 23, 2017.
- Has FDA refused shipments from SC PlantExtrakt?
- No FDA import refusals for SC PlantExtrakt appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is SC PlantExtrakt's FEI number?
- SC PlantExtrakt's FDA Establishment Identifier (FEI) is 3010698715.
- Can shipments from SC PlantExtrakt still enter the U.S.?
- Shipments of uti relief; silver birch; common fig; black currant; allergy relief; anxiety relief; digestive relief; earache relief; flu relief from SC PlantExtrakt can be detained without physical examination under Import Alert 99-39; 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.