Food Recall Check
Class I · High risk Terminated Initiated Feb 7, 2017 (10 years ago)

Xanthium & Siler Combo recall

Recalled by Kingsway Trading Inc · Brooklyn, NY, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Presence of Ephedrae Herba (ma huang), a FDA Banned Ephedra Alkaloid

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Xanthium & Siler Combo (Bi Yan Pian) DIETARY SUPPLEMENT, Net cont: 100 tablets (300mg each), Net Wt. 1.06oz (30g)

Quantity: 100 cases/100 bottles/100 tablets

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

lot # 020115 Exp 01/2020 lot # 040113 Exp 03/2017

Where it was sold

Arizona Colorado Connecticut Delaware Florida Georgia Illinois Indiana Massachusetts Maryland Missouri New Jersey New York Oregon Pennsylvania Texas Virginia

FDA's distribution note: 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.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Kingsway Trading Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 7, 2017
In FDA report of
Mar 22, 2017
Terminated
Jun 25, 2018
FDA recall number
F-1577-2017 · event 76404
Official record
FDA enforcement report search

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