FDA recall record

Jimmy Weber Red Zone Xtreme 3000 Capsules, Dietary Supplement Product, 1 count blister pack recall — FDA D-0625-2018

Marketed without an Approved NDA/ANDA; FDA analysis found this product to contain undeclared Tadalafil, an FDA approved drug for the treatment of erectile…

Class Iclassification
D-0625-2018official record ID
Apr 4, 2018report date

Recall record at a glance

Official recordD-0625-2018
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmJimmy Weber
Report dateApr 4, 2018
Recall initiation dateMar 8, 2018
Quantity315 capsules
LocationLos Angeles, CA, United States

Official product description

Red Zone Xtreme 3000 Capsules, Dietary Supplement Product, 1 count blister pack, UPC 8 91656 00200 9, Exp Date 12/31/2021

Why the product was recalled

Marketed without an Approved NDA/ANDA; FDA analysis found this product to contain undeclared Tadalafil, an FDA approved drug for the treatment of erectile dysfunction.

Distribution information

Product was distributed online via eBay.

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: E-Mail.

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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