Two intimacy products often used by the over 40 crowd have been recalled.
Vaginal dryness is one of the main complaints of premenopausal and menopausal women, so they often use lubrication to ease the pain during intercourse. It’s important for those using lubricants to know that Johnson & Johnson has recalled K-Y Liquibeads Vaginal Moisturizer.
McNeil PPC, Inc., the company that makes K-Y, has assured customers that there is nothing wrong with the K-Y Liquibeads Vaginal Moisturizer. Instead, the company must recall the product due to clearance issues with the FDA.
The FDA reports that they have received over 200 complaints about the Liquibeads having an unusual texture and not dissolving.
There is no call for consumers to return the product.
CRM Laboratories has announced the recall of X-ROCK 3 Day Pill For Men and Z-ROCK products sold as an all natural male enhancement drug.
The product contains Sildenafil, an active pharmaceutical ingredient in a FDA approved drug used to treat erectile dysfunction (ED). That means the X-ROCK and Z-ROCK products fall into the “unapproved new drugs” category.
“These undeclared active ingredients pose a threat to consumers because sildenafil and hydroxythiohomosildenafil may interact with nitrates found in some prescription drugs (such as nitroglycerin) and lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates,” reports the FDA.
The affected products include:
X-Rock 3 Day Pill for Men back panel may read Distributed by XRock Industries PO Box 120863 Ft. Lauderdale, FL 33312 or MATE Enterprises 1020 N. Venetian Drive Miami, Florida 33139 www.XRockHim.com (888) XROCK-HIM).
Z-Rock All Natural Male Supplement back panel will read Distributed By XRock Industries PO Box 120863 Ft. Lauderdale, FL 33312 www.ZrockUSA.com 877-976-2563.
The FDA recommends that consumers stop taking the products immediately and call 305-587-9830 to receive instructions on returning the products for a refund.