FDA Abandons Plan to Test for Asbestos in Cosmetics, Averting Potential Cancer Risk
The US Food and Drug Administration (FDA) is set to kill its proposal requiring testing for toxic asbestos in talc-based cosmetics, a move that has left health campaigners stunned. The plan was signed by Robert F Kennedy Jr, leader of the "Make America Healthy Again" movement, which aims to eliminate toxins like asbestos from food, medicine, and personal care products.
The FDA's decision comes despite growing evidence linking asbestos exposure to cancer. Asbestos is a known human carcinogen that has been linked to approximately 40,000 deaths annually. Despite this, companies have been allowed to rely on testing methods that can detect only some, but not all, asbestos fibers.
Cosmetic giant Johnson & Johnson, which discontinued US talc-based baby powder sales in 2020 amid mounting public pressure and nearly 38,000 lawsuits, is facing billions of dollars in settlements for allegedly knowingly poisoning consumers. The company's high-profile cases highlight the risks associated with asbestos contamination in personal care products.
Regulating asbestos has been a contentious issue, with an initial 1989 EPA ban being quickly overturned by a court. Efforts to pass similar bans have failed over the years, despite clear dangers and widespread use.
Critics argue that the FDA's decision is misguided, citing the potential for "unintended consequences" that may favor companies rather than public health. Environmental Working Group Vice-President Scott Faber described the move as "tragic" and noted that Kennedy Jr, who signed the order, has a history of advocating for people's health.
In its notice announcing the withdrawal of the proposed rule, the FDA cited concerns about potential "unintended consequences" in relation to pharmaceutical companies. However, this decision leaves many wondering whether the agency prioritized corporate interests over public health and safety.
The US Food and Drug Administration (FDA) is set to kill its proposal requiring testing for toxic asbestos in talc-based cosmetics, a move that has left health campaigners stunned. The plan was signed by Robert F Kennedy Jr, leader of the "Make America Healthy Again" movement, which aims to eliminate toxins like asbestos from food, medicine, and personal care products.
The FDA's decision comes despite growing evidence linking asbestos exposure to cancer. Asbestos is a known human carcinogen that has been linked to approximately 40,000 deaths annually. Despite this, companies have been allowed to rely on testing methods that can detect only some, but not all, asbestos fibers.
Cosmetic giant Johnson & Johnson, which discontinued US talc-based baby powder sales in 2020 amid mounting public pressure and nearly 38,000 lawsuits, is facing billions of dollars in settlements for allegedly knowingly poisoning consumers. The company's high-profile cases highlight the risks associated with asbestos contamination in personal care products.
Regulating asbestos has been a contentious issue, with an initial 1989 EPA ban being quickly overturned by a court. Efforts to pass similar bans have failed over the years, despite clear dangers and widespread use.
Critics argue that the FDA's decision is misguided, citing the potential for "unintended consequences" that may favor companies rather than public health. Environmental Working Group Vice-President Scott Faber described the move as "tragic" and noted that Kennedy Jr, who signed the order, has a history of advocating for people's health.
In its notice announcing the withdrawal of the proposed rule, the FDA cited concerns about potential "unintended consequences" in relation to pharmaceutical companies. However, this decision leaves many wondering whether the agency prioritized corporate interests over public health and safety.