Huisong Pharmaceuticals
FDA import alert and refusal historyHangzhou, ChinaFEI 3009881519
As of October 26, 2026, Huisong Pharmaceuticals (Hangzhou, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for panax ginseng (extract powder), published by FDA on July 31, 2018, and has 4 FDA import refusals 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
- Mushroom, shiitake, pieces and stems, sliced · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Huisong Pharmaceuticals
6 records, newest first. Each line links to the FDA page it came from.
2021
2020
2018
- Import alert listingListed on Import Alert 99-08red listPanax Ginseng (Extract powder)Source
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
- 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.
- PESTICIDE2 refused lines
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 Huisong Pharmaceuticals
- Is Huisong Pharmaceuticals on an FDA import alert?
- Yes. As of October 26, 2026, Huisong Pharmaceuticals is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for panax ginseng (extract powder); FDA published the listing on July 31, 2018.
- Has FDA refused shipments from Huisong Pharmaceuticals?
- Yes. FDA refused 4 shipment lines from Huisong Pharmaceuticals between January 31, 2020 and December 21, 2021. The most recent, on December 21, 2021, was mushroom, shiitake, pieces and stems, sliced, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Huisong Pharmaceuticals's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 2 lines) and PESTICIDE (pesticide chemical residue, 2 lines).
- When was Huisong Pharmaceuticals last inspected by FDA?
- FDA's most recent inspection of Huisong Pharmaceuticals with a final classification is dated May 13, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Huisong Pharmaceuticals's FEI number?
- Huisong Pharmaceuticals's FDA Establishment Identifier (FEI) is 3009881519.
- Can shipments from Huisong Pharmaceuticals still enter the U.S.?
- Shipments of panax ginseng (extract powder) from Huisong Pharmaceuticals 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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