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X-ROCK Recall Lawsuit

A Fort Lauderdale, FL establishment is now recalling X-ROCK dietary supplements because they were found to contain an ingredient that may interact with nitrates and lower blood pressure to dangerous levels. X-ROCK was distributed to wholesalers and retail to the consumer via Internet orders. Individuals with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates, and men with these conditions may seek products like X-ROCK to enhance sexual performance.

X-ROCK Dietary Supplement Recall Update 7/20/12: CRM Laboratories is now recalling X-ROCK 3 Day Per Pill For Men and Z-ROCK dietary supplements sold between October 2011 and April 2012 because they contain an analogue of an ingredient found in an FDA-approved drug. The undeclared ingredients in question pose a threat to consumers because they may interact with certain medications and lower blood pressure to dangerous levels. Click here to learn more.

Dietary Supplement Lawsuit Update 6/7/12: In a recent landmark lawsuit, a leading online dietary supplement retailer pled guilty to selling products laced with steroids and agreed to pay a hefty $7 million fine. Many legal experts believe the case will set a new precedent for cracking down on vendors of adultered products. Click here for more information.

Free X-ROCK Lawsuit Evaluation: If you or a loved one has suffered a serious injury you feel may have been caused by X-ROCK, you should contact our law firm immediately. You may be entitled to compensation by filing a suit against the manufacturer of X-ROCK and we can help.

What’s the problem with X-ROCK?

April 19, 2012 – The U.S. Food & Drug Administration (FDA) issued a press release today informing the public that XROCK INDUSTRIES is currently recalling all lot numbers of the following product because they may contain an analogue of an ingredient in an FDA-approved drug:

  • X-ROCK dietary supplement – UPC 0030950792 – packaged individually in one capsule blister cards

Analytical tests conducted by the FDA concluded that this product contains hydroxythiohomosildenafil, an analogue of sildenafil, which is the active ingredient erectile dysfunction drugs like Viagra.

Hydroxythiohomosildenafil is structurally similar to sildenafil, and is expected to cause the same side effects and adverse reactions. These undeclared active ingredients have been shown to have the potential to interact with nitrates found in certain prescription medications such as nitroglycerin, and may lower blood pressure to dangerous levels. Additionally, both hydroxythiohomosildenafil and sildenafil may cause more moderate side effects such as headaches and flushing.

Consumers who have X-ROCK capsules included in this recall in their possession should discard them immediately or return them to the place of purchase for a full refund. If you are experiencing any serious side effects you feel may be related to taking this drug, you should contact your physician immediately. To date, there have been no illnesses reported in connection with this recall.

Need More Info?

Click on the links below if you’d like additional information on these topics from Schmidt & Clark, LLP:

Do You Have an X-ROCK Lawsuit?

The Product Liability & Defective Drug Litigation Group at our law firm is an experienced team of trial lawyers that focus on the representation of plaintiffs in X-ROCK lawsuits. We are handling individual litigation nationwide and currently accepting new X-ROCK side effects cases in all 50 states.

Free X-ROCK Lawsuit Evaluation: If you or a loved one has suffered a serious injury you feel may have been caused by X-ROCK, you should contact our law firm immediately. You may be entitled to compensation by filing an X-ROCK injury suit and we can help.

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