FDA recall record

Chaotic Labz MAYHEM capsules, Proprietary Blend 525 mg, Dietary Supplement, 60-count recall — FDA D-0314-2015

Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared dexamethasone and cyproheptadine which are FDA approved drugs…

Class IIclassification
D-0314-2015official record ID
Dec 31, 2014report date

Recall record at a glance

Official recordD-0314-2015
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmChaotic Labz
Report dateDec 31, 2014
Recall initiation dateNov 14, 2014
Quantity990 bottles
LocationAtkins, AR, United States

Official product description

MAYHEM capsules, Proprietary Blend 525 mg, Dietary Supplement, 60-count bottles, Chaotic-Labz, UPC 6 28586 67805 7.

Why the product was recalled

Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared dexamethasone and cyproheptadine which are FDA approved drugs making this product an unapproved drug.

Distribution information

Nationwide.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

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

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