Consumers who purchased Dermatend Original and Dermatend Ultra to remove moles and warts should immediately discontinue use and consult their physician
San Diego, CA (PRWEB) September 05, 2014
AttorneyOne.com, a recognized authority on law, update the website daily regarding all the latest information from the FDA on Dermatend Original and Dermatend Ultra.
The US FDA announced on September 2, that Solace International, Inc. is recalling all lots of Dermatend Original and Dermatend Ultra due to safety concerns. Dermatend Original and Dermatend Ultra products are used to remove moles, skin tags, and warts.
According to the FDA announcement, the reason for the recall is that the product, not FDA approved, has not been shown to be safe and effective. Moreover, if the product is used instead of seeking medical attention, this could result in delayed diagnosis of serious conditions, including cancer.
Taking into consideration the latest developments, AttorneyOne.com monitor daily and update the website providing accurate information on all relevant FDA safety alerts. Sean Burke, director of Media Relations at AttorneyOne.com, adds, “We are determined to keep an eye on FDA announcements concerning Dermatend Original and Dermatend Ultra and inform the public. For that reason," he continues, "our focus should squarely fall on updating people on these safety alerts and getting the word out.”
As the FDA recommends, “Consumers who purchased Dermatend Original and Dermatend Ultra to remove moles and warts should immediately discontinue use and consult their physician.” And the Agency adds, “Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.”
AttorneyOne.com has further information on Dermatend Original and Dermatend Ultra at the website including the latest major drug, food, and medical products law news.
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