FDA recall record

Fabscout Entertainment Evil Root 1200 mg, supplied in 6 capsules per bottle, Manufacturer recall — FDA D-376-2014

Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil

Class Iclassification
D-376-2014official record ID
Dec 25, 2013report date

Recall record at a glance

Official recordD-376-2014
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmFabscout Entertainment, Inc.
Report dateDec 25, 2013
Recall initiation dateAug 14, 2013
Quantity32 bottles of 6 capsules each
LocationFt Lauderdale, FL, United States

Official product description

Evil Root 1200 mg, supplied in 6 capsules per bottle, Manufacturer: Tibet Shengyang Health Medicine Co.,Ltd. Address: No. 98, Min zu Road, Lhasa

Why the product was recalled

Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil

Distribution information

CA, FL and UT

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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