Kingsway Trading Xanthium & Siler Combo Dietary Supplement Recall: Ephedra Alkaloid Hazard
Kingsway Trading recalls Xanthium & Siler Combo (Bi Yan Pian) dietary supplement due to presence of FDA-banned ephedra alkaloid. Consumers should stop using affected lots.
Stop using this now
Presence of Ephedrae Herba (ma huang), a FDA Banned Ephedra Alkaloid
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What happened, in plain English
Kingsway Trading is recalling Xanthium & Siler Combo (Bi Yan Pian) dietary supplements because they contain ephedra alkaloids banned by the FDA. This poses a risk of serious health effects due to the banned substance. Read more at govinfonow.com/recall/22338-kingsway-trading-xanthium-siler-combo-dietary-supplement-recall-ephedra-alkaloid.
Source Summary by GovInfoNow · govinfonow.com/recall/22338-kingsway-trading-xanthium-siler-combo-dietary-supplement-recall-ephedra-alkaloid · Updated October 8, 2026 · FDA enforcement record: FDA #F-1577-2017
Cite this page
“Kingsway Trading Xanthium & Siler Combo Dietary Supplement Recall: Ephedra Alkaloid Hazard.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22338-kingsway-trading-xanthium-siler-combo-dietary-supplement-recall-ephedra-alkaloid. Based on FDA recall #F-1577-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1577-2017%22&limit=1).
Why it’s dangerous
Ephedra alkaloids are banned by the FDA because they can cause serious health issues including heart problems, high blood pressure, and other dangerous side effects. The presence of these substances in the dietary supplement makes it unsafe for consumption.
Who’s affected
Anyone who owns or uses the recalled dietary supplement, particularly those who have purchased it from the listed lots. People with pre-existing health conditions may be at higher risk.
How to tell if you have this one
Check the product label for the lot numbers: 020115 (expires 01/2020) or 040113 (expires 03/2017). The product is a dietary supplement containing 100 tablets of 300mg each.
- Brand
Kingsway Trading- Category
Food
What to do — step by step
Stop Using Now
Immediately stop using the recalled Xanthium & Siler Combo (Bi Yan Pian) dietary supplement if you have the affected lot numbers.
Where it went and when
Where it was distributed
Distributed in 17 states.
FDA distribution: “MA, NJ, NY, IL, MD, FL, MO, TX, IN, GA, DE, CO, VA, PA, CT, OR, VA, AZ, Through asianl herb stores, acupuncture clinics and asian supermarkets.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Colorado, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Maryland, Massachusetts, Missouri, New Jersey, New York, Oregon, Pennsylvania, Texas, Virginia.
Recall timeline
FDA terminated this recall 17 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1577-2017 (February 7, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1577-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.