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Tuesday, 13 April 2010

recall for stud capsuleStud Capsule for Men Recalled Due to Containing Sildenafil

The FDA has informed Kanec USA Inc. through it’s representatives that it had conducted laboratory analysis of one of it’s products called Stud Capsule for Men. In this analysis the FDA had found the product to contain Sildenafil, an FDA approved drug for erectile dysfunction (ED), making Stud Capsule for Men a new unapproved drug. The sample was taken from lot number 060607-01/060108-01 Exp 6-2013.

This product is now a threat to consumers who may be on other prescription medications. Consumers will be unaware of this threat because Sildenafil will not be marked on the label. If this product mixes with prescriptions for diabetes, high cholesterol, heart disease, and high blood pressure, it could cause dangerously low blood pressure resulting in death. People with these conditions maybe taking nitrates, which is the danger with Sildenafil.

 

And because many men that maybe taking nitrate often suffers from ED seek out solutions to help with their sexual performance. So you can see the related danger of the situation.

stud capsule for men recalledBecause of this Kanec USA Inc. has announced a voluntary nationwide recall of this product (Stud Capsule for Men). This product is sold in blister packs containing 24 individual capsules. The lot numbers and expiration date appear on the seal of the package. Consumers with lot and expiration number 060607-01/060108-01 Exp 6-2013 should stop using them immediately.

If you are experiencing any side affects while using this product you should contact a physician immediately. Consumers are also encouraged to report these adverse side affects to the FDA Med Watch Program .

Kanec USA Inc is asking consumers to either return said products to the retailers in which they were purchased, or they can return them directly to:

Kanec USA Inc.
5061 South State Road 7, U602
Davie, Florida, 33314
Ph. 954-583-5840
Fx. 954-583-5885

Kanec USA Inc. wants it’s consumers to know it is working very closely with the FDA in this recall process and apologizes for any inconveniences it may have caused in this oversight. It expresses its concerns for the health and well being of the people using its products and assures everyone that it is taking the necessary steps to rectify this problem. Its quality control is on both the raw materials and the finished product is very stringent, but its testing protocols never tested for the presence of Sildenafil.

 
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