Tendex recalls NATURECT Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5, 10, 20, and 40- count bottles, Dist

Recalled May 28, 2014 · FDA recall D-1346-2014 · Tendex

Hazard

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to contain undeclared active ingredient, tadalafil, thus making these products unapproved drugs. · FDA Class I

Units

unknown

Sold at

Nationwide.

Description

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to contain undeclared active ingredient, tadalafil, thus making these products unapproved drugs.

Product

NATURECT Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5, 10, 20, and 40- count bottles, Distributed by P-Boost, Los Angeles, CA 900466

Manufacturer(s)

Tendex

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →