The FDA urges consumers and healthcare providers to report adverse reactions from tattoos, permanent makeup, and temporary tattoos, as well as problems with tattoo removal.Ĭonsumers and healthcare providers can report problems to MedWatch, the FDA’s problem-reporting program, calling 1-80, or by contacting the nearest FDA consumer complaint coordinator. The FDA has also established Import Alert #53-19: Detention Without Physical Examination of Henna Based Skin Color.The inks associated with this outbreak were voluntarily recalled by the company that marketed them in 2004.įor details on all tattoo ink recalls, please see our Recalls & Alerts Page. Additionally, in 20, the FDA became aware of more than 150 reports of adverse reactions in consumers to certain permanent makeup ink shades.In the fall of 2011, a firm initiated a recall for its product due to lab test results finding traces of bacteria in the ink.In the spring of 2012, the FDA received reports of infections from contaminated inks, resulting in their recall and market withdrawal.In the summer of 2014, the FDA notified consumers of the voluntary recall of tattoo inks and needles due to confirmed bacterial contamination. ![]()
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