The Beast recalled over undeclared sildenafil

Recall date

May 6, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Stiff Boy LLC recalls The Beast, The Beast can be taken under the situation of Heart disease and even after drinking, 4600 mg X 4 Capsules pe…

Recall number

D-1321-2019

FDA classification

Class I

Brand / firm

Stiff Boy LLC

Sold / distributed

Nationwide

Why it was recalled

Marketed without an Approved NDA/ANDA: The Beast contains undeclared sildenafil which was discovered through FDA analysis.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

The Beast, The Beast can be taken under the situation of Heart disease and even after drinking, 4600 mg X 4 Capsules per packet.