Keime Inc. dba Barry's Vitamins - Virility Max FDA Recall

 

 

Keime Inc. of Florida, released a statement issuing a voluntary recall of their male enhancement product, Virility Max. After a lab analysis done by the FDA, the product tested positive for sulfoaildenafil, an analog of sildenafil. The analysis' results meant Virility Max is an unapproved drug.

 

The lot number in question is Lot 10090571. If you are in possesion or currently using Virility Max, it is important to immediately stop using the product. The male enhancement product, Virility Max is sold in plastic white bottles and distributed in 10 counts. For more information on the FDA Recall of Virility Max, read here.

Superior Metabolic Technologies Inc. - Uprizing 2.0 - FDA Recall

Superior Metabolic Technologies Inc of Marietta, Georgia is voluntarily recalling their product, Uprizing 2.0. This FDA recall is for all lots of the product, Uprizing 2.0. Tests results have shown that Uprizing 2.0 contains superdrol which is a synthetic steroid, making it an unapproved new drug.

The discovery of superdrol has led to the recall of the product by FDA and Superior Metabolic Technologies. If you have purchased or are in possession of Uprizing 2.0, it is suggested to immediately stop using it. It's distribution in the United States spread from health food stores in states, Alabama, Arizona, California, Georgia, Mississippi, New Jersey, South Carolina and Texas.

Patrons who have purchased this product are asked to return it to the company and receive a full refund. Uprizing 2.0 was packages in a black plastic bottle with a red, silver and black label. The bottle contained 90 capsules as well. For more information on the FDA recall of Uprizing 2.0, read here.

VIA XTREME - Global Wellness, LLC. - EXPANDED - FDA Recall

Global Wellness, LLC. Hollywood, FL expanded its voluntary nationwide recall of VIA XTREME ULTIMATE SEXUAL ENHANCER DIETARY SUPPLEMENT FOR MEN to the consumer level to now include lot A032111.

The distribution of this male enhancement product was throughout the United States, Puerto Rico, Canada and Barbados.

This male enhancement product is being sold in a bottle containing six blue capsules in each package. Global Wellness, LLC, Hollywood Florida is the company name listed on the packaging.

The expanded FDA Recall now includes these lot numbers # 809013, 806030, and A032111.

For more information about the Expanded FDA Recall on Global Wellness, LLC. Via Xtreme Ultimate Sexual Enhancer Dietary Supplement, read here.

Global Wellness, LLC. - VIA XTREME ULTIMATE SEXUAL ENHANCER DIETARY  SUPPLEMENT FOR MEN - FDA RECALL

 

Global Wellness, LLC. Hollywood, FL have released a statement and voluntary recall along with the FDA of VIA XTREME ULTIMATE SEXUAL ENHANCER DIETARY SUPPLEMENT FOR MEN to the consumer market. The Lots being recalled are 806030 and 809013. The distribution of this male enhancement product was throughout the United States, Puerto Rico and Canada.

 

The FDA lab breakdown of Lots 806030 and 809013 conducted by the FDA found that said product contains sulfosildenafil and dimethylsildenafil analogs of sildenafil and sulfoaildenafil methanesulfonate.  This makes Via Xtreme Ultimate Sexual Enhancer Dietary Supplement for Men an unapproved drug. Active ingredients are not listed on the product label as well. Interaction with the undeclared drug can cause conflicting affects to the consumer.

 

An interaction is possible with the Via Extreme Ultimate Sexual Enhancer Dietary Supplement and nitrates found in prescription drugs such as nitroglycerin and it has the potential to lower blood pressure. Furthermore, patrons who suffer from high cholesterol, heart disease, diabetes and high blood pressure take nitrates. Other common side effects are flushing and headaches.

 

For more information about the FDA Recall on Global Wellness, LLC. Via Xtreme Ultimate Sexual Enhancer Dietary Supplement, read here.

Ethos Environment, Inc. - Regenerect - FDA Recall

After a conclusive lab analysis by the FDA, it has been confirmed that the presence of Sulfoaildenafil, an ingredient of an FDA-approved drug used in practice to treat erectile dysfunction. Ethos Environmental, Inc. who distributes Regenerect poses a threat to patrons who are prescribed or are taking nitrates that are found in prescription drugs. The side effect with this interaction it that it can cause blood pressure to drop to dangerous levels. Also at risk are patrons with diabetes, high cholesterol, high blood pressure and heart disease.

If you are in possession of this product and the lot numbers match, it is advised to discontinue use immediately. Ethos Environmental, Inc., Regenerect will refund any product that is returned to the company directly.

Read more information on the FDA recall of Regenerect here.

AVNS, Inc. - THE BEST Enhancer - FDA Recall

 

The FDA and AVNS, Inc declared today a voluntary recall of THE BEST Enhancer male supplement. Their manufacturer, Drive Total Energy informed AVNS Inc that the FDA's lab examination found Sulfoaildenafil, an equivalent of Sildenafil. Sildenafil is an approved drug by the FDA to treat Erectile Dysfunction in males. This composition makes these products by AVNS Inc unapproved new drugs. Furthermore there is no listing of the active ingredient on the product label.


The FDA has surmised that this product comes from an unspoken ingredient and could pose a threat to a patrons health. The use of prescription drugs and the THE BEST Enhancer may interact and cause dangerously low levels of blood pressure. Men who are seeking help for Erectile Dysfunction and are diabetic are at greatest risk of this interaction between prescription drugs and THE BEST Enhancer male enhancement product. Others at risk are subject's with high cholesterol, heart disease, and high blood pressure. Read more about the FDA Recall on AVNS, Inc, Recall.


The FDA and AVNS, Inc and advise customers who are in possession of this male enhancement product to refrain their use and return the supplement to their place of purchase for a complete refund.

USA Far Ocean Group Inc - X-Hero - Male Enhancer - FDA Recall

The FDA and USA Far Ocean Group Inc., have issued a voluntary recall for the male enhancement supplements, X-Hero and Male Enhancer. A lab examination performed by the FDA found that X-Hero's active ingredient is sulfosidenafi, which the FDA deemed an unapproved drug. The FDA lab examination of Male Enhancer shows the product contains tadalafil, which the FDA cited as unapproved drug as well.


The FDA has concluded that both products pose a great risk to those who take prescription drugs because they may interact the X-Hero or Male Enhancer product. The interaction with nitrates like nitroglycerin is a health concern to anyone trying to treat their erectile dysfunction problem. The threat this poses to someone's health is low blood pressure to dangerous levels. Men suffering from erectile dysfunction are at risk to such conditions as these are common with person's with diabetes. The side effects that FDA found may be caused from tadalafil or sulfosildenafil are commonly flushing and headaches. Read more about the FDA recall on USA Far Ocean Group Inc. FDA Recall.


The following packages of X-Hero and Male Enhancer products are included in this voluntary recall:


X-Hero with English Label 10 ct 689087070995

X-Hero with English Label 8 ct 689076499255

X-Hero with Chinese/English Label 8 ct 689076499255

X-Hero with English Label 1 ct no upc code

Male Enhancer 60 ct 982010061205


These products are for sale nationwide through various points of purchase like retail locations, internet sales and mail ordering. The FDA would advise customers who have purchased the X-Hero or Male Enhancer products to stop use of it right away. Contact your physician if problems were encountered related to the use of this male enhancement product.

Black Ant FDA Recall

 

The FDA has issued a recall and released a statement encouraging patrons not to use or purchase Black Ant male enhancement product. Black Ant is a male enhancement product product sold on numerous web retail sites.

The maker of the product states that it is "natural sex enhancer" and has "no known side effects."

An FDA Lab analysis found that the male enhancement product, Black Ant contains sildenafil. The analysis further showed that the tested product contained three times the FDA approved dosage for sildenafil.

It is advised that patrons immediately stop the use or purchase of Black Ant.

For more information on the Black Ant sexual enhancer FDA recall, read here.

Fake Extenze - FDA Recall

The FDA and BIOTAB NUTRACEUTICALS, INC have issued a recall for the Male Enhancement Supplement Extenze. The Extenze Men's Regular was marketed as a Dietary Supplement for sexual enhancement on television and throughout stores.  The Food and Drug Administration (FDA) found that the lab analysis of one lot of the products tested by the FDA found that the product contains undeclared Tadalafil and Sildenafil, an FDA-approved drug used for the treatment of male Erectile Dysfunction (ED), making the fake counterfeit lots of Extenze an unapproved drug.  Read more about the FDA Recall on Fake Extenze Men's Regular FDA Recall.

The Recall included the following lots: Extenze lot 0709241 contains tadalafil and sildenafil was recalled, and Extenze lot 0509075 contains tadalafil and sibutramine and was recalled. The counterfeit Extenze can be found at retail male enhancement product stores nationwide in the form of carded four-packs (Extenze lot 0709241) and in the form of a box of thirty Extenze  tablets divided into two fifteen tablet blister packs (Extenze lot 0509075).

Stud Capsule for Men - FDA Recall

The FDA and Kanec USA, Inc have issued a recall for the Stud Capsule For Men Male Enhancement Supplement. The Food and Drug Administration (FDA) that lab analysis of one lot of the Stud Capsule for Men products tested by the FDA found that the product contains undeclared Sildenafil, an FDA-approved drug used for the treatment of male Erectile Dysfunction (ED), making Stud Capsule for Men an unapproved drug.  Read more about the FDA Recall on Stud Capsule for Men. This would be a concern for people with Diabetes or High Blood Pressure because it would interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels.

The Recall included the following lots: Stud Capsule For Men Lot #060607-01/060108-01 Exp 6-2013

The FDA Recall of Stud Capsule for Men by Kanec USA recommends that consumers who have Stud Capsule For Men Lot 060607-01/060108-01 Exp 6-2013 in their possession should stop using them immediately.

Rock Hard Extreme and Passion Coffee Dietary Supplements - FDA Recall

Drive Total Energy announced the recall of the of male enhancement supplements Rock Hard Extreme and Passion Coffee Dietary Supplements. Drive Total Energy is conducting the voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analyses found that the products to contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used in the treatment of male Erectile Dysfunction making Rock Hard Extreme and Passion Coffee an unapproved drug.  

Some of the ingredients possibly pose a threat to the consumers because of the interaction of the analogue with some prescription drugs (such as nitroglycerin) which may lower ones blood pressure to dangerously high levels. Consumers with diabetes, high blood pressure, high cholesterol, heart disease or other medical issues and who often take prescription drugs are at risk of heart failure. Read more about the FDA Recall on Rock Hard Extreme and Passion Coffee.

Man Up Now - FDA Recall

The FDA has issued a recall for the Male Enhancment Product or Male Enlargement Pills Man Up Now.  The Man Up Now capsules are marketed as a Dietary Supplement for sexual enhancement.  The FDA had determined that there is an unknown ingredient as well as a chemical called sulfoaildenafil.  This is actually similar to an ingredient found in Viagra.  The FDA had determined that you need to have a perscription for any product that uses this chemical. Read more about the FDA Recall on Man Up Now.

TimeOut Capsules - FDA Recall

The FDA has issued a recall for the Male Enhancement Product TimeOut Capsules.  TimeOut Capsules was marketed as a Dietary Supplement for sexual enhancement.  The FDA analyzed TimeOut and determined that it contains hydroxythiohomosildenafil, a chemical similar to sildenafil, the active ingredient in Viagra. Like sildenafil, this chemical may interact with prescription drugs such as nitrates, including nitroglycerin, and cause dangerously low blood pressure. When blood pressure drops suddenly, the brain is deprived of an adequate blood supply which can lead to dizziness or lightheadedness.  Read more about the FDA Recall on TimeOut Capsules.

Magic Power Coffee - FDA Recall

The FDA has issued a recall for the Male Enhancment Supplement Magic Power Coffee. Magic Power Coffee was marketed as a Dietary Supplement for sexual enhancement.  The Food and Drug Administration (FDA) that lab analysis of one lot of the product by the FDA found that the product contains undeclared hydroxythiohomosildenafil, similar in structure to Sildenafil, an FDA-approved drug used for the treatment of male Erectile Dysfunction (ED), making Magic Power Coffee an unapproved drug.  Read more about the FDA Recall on Magic Power Coffee.

Stiff Nights & RockHard Weekend - FDA Recall

 

The FDA has issued a recall for the Male Enhancement Pills Stiff Nights and RockHard Weekend.  Stiff Nights and RockHard Weekend capsules are marketed as a Dietary Supplement for performance enhancement. The presence of sulfoaildenafil makes RockHard Weekend and Stiff Nights unapproved drugs. The undeclared drug ingredient, sulfoaildenafil, may interact with prescription drugs known as nitrates, including nitroglycerin, and cause dangerously low blood pressure.  Read more about the FDA Recall on Stiff Nights and RockHard Weekend.

Zencore Plus - FDA Recall

The FDA has issued a recall for the Male Enhancement Pill or Male Enlargement Product Zencore Plus. Zencore capsules are marketed as a Dietary Supplement for performance enhancement. FDA tests of Zencore Plus samples found the product to contain benzamidenafil which is a newly discovered PDE5 inhibitor. If the user had an undiscovered illness, the use of Zencore Plus could be life threatening. Read more about the FDA Recall on Zencore.