FDA Warns Against Use of Injectable Silicone for Body Contouring and Enhancement

Public Service – Mankato Times

ST PAUL, MINN. — Today, the U.S. Food and Drug Administration (FDA) issued a Safety Communication titled, “The FDA Warns Against Use of Injectable Silicone for Body Contouring and Enhancement.” The FDA is alerting the public and health care providers that the FDA has not approved injectable silicone for large-scale body contouring or enhancement, and that these kinds of uses can lead to serious injury, permanent scarring or disfigurement, and death.

The FDA is aware of cases where patients have received injectable silicone for body contouring purposes, such as gluteal or breast enhancement (“butt fillers” or “breast fillers”), by unqualified providers posing as doctors or licensed healthcare practitioners in non-clinical settings such as residential homes or hotels. The FDA is aware that some injectors have falsely told consumers they were receiving an FDA-approved dermal filler, but consumers were instead injected with silicone.

Injectable silicone is permanent, with side effects that can occur right after the injection and up to years after treatment. Silicone spreads and migrates easily inside the body, which may worsen adverse events and make surgical attempts to remove the silicone oil more difficult or impossible. Silicone, when injected into areas with many blood vessels such as the buttocks, can travel to other parts of the body and block blood vessels in the lungs, heart, or brain. This can result in permanent damage to those tissues and lead to stroke or death.

Surgery to remove large-scale injectable silicone may present additional risks and serious complications, and may not entirely rid the body of the silicone. Multiple medical and surgical interventions are sometimes needed to treat symptoms years after initial injection; even then, patients may continue to experience ongoing pain, infection, and scarring and permanent disfigurement requiring ongoing treatment.

Recommendations for Consumers: Injectable Silicone

  • Do not get injectable silicone or any type of filler material for large-scale body contouring or enhancement. This means you should never get an injectable filler as a breast filler, “butt filler,” or filler for spaces between your muscles. The FDA is aware of serious medical problems and multiple deaths associated with such use. (See the Summary of Problem and Scope section above for more information.)
  • Know that there are no FDA-approved injectable silicone products for body contouring, or to increase the size of areas such as the breasts or buttocks. The only approved uses for dermal fillers are available on the FDA Dermal Fillers website.
  • Seek medical attention immediately if you experience problems such as difficulty breathing, chest pain, signs of a stroke (including sudden difficulty speaking, numbness or weakness in your face, arms, or legs, difficulty walking, face drooping, severe headache, dizziness, or confusion) after receiving injectable silicone, as it may be a life-threatening situation. Be sure to let your health care provider know you have had silicone injections.
  • Seek appropriate medical care, such as from a licensed board-certified plastic surgeon, if you have had silicone oil injections and are experiencing side effects such as pain, hardening of the skin, lumps, or infections.
  • If you believe you have been offered or have received injectable silicone for body contouring from an unlicensed provider, you are encouraged to use the FDA website to report suspected criminal activity.
  • If you are considering a body enhancement or body contouring procedure, only see a licensed health care provider who has appropriate training and experience (e.g., plastic surgeon).

Recommendations for Consumers: FDA-Approved Dermal Fillers

  • Before deciding to have any sort of filler injections, talk with your licensed health care provider about appropriate treatment injection sites and the risks associated with the procedure as well as the product being injected. Know that FDA-approved dermal fillers are not indicated for everyone.
  • Only get FDA-approved dermal fillers injected by licensed health care providers. These health care providers should have appropriate training and experience and should be knowledgeable about the anatomy at and around the injection site.
  • When getting any sort of injectable filler, ask your health care provider for the FDA-approved product brochure and patient labeling.
    • Ask questions and read and discuss the patient labeling for the specific filler you are receiving.
    • Check the FDA website on approved dermal fillers prior to receiving treatment to confirm that the product has been approved by the FDA.
    • Confirm the credentials of your health care provider and the material being injected, and avoid receiving treatment outside of a medical clinic.

Recommendations for health care providers

  • Be aware that injectable silicone is not approved for large-scale body contouring or enhancement, and serious adverse events have been reported. The FDA recommends that you do not inject silicone to achieve breast, muscle, or buttocks enhancement.
  • Be aware that:
    • The use of silicone oil outside intraocular ophthalmic use is not approved by the FDA.
    • Silicone injections used for body enhancement have resulted in serious injuries or death.
    • When treating patients after injections for body contouring, the type of material used may be unknown.
    • When treating patients who have received silicone injections, the material injected may migrate during revision surgery, which may worsen adverse events and make attempts to remove the injectable silicone oil difficult, incomplete, or impossible.
  • Educate health care facility staff on how to quickly identify and assist patients who report signs and symptoms of complications from injectable silicone. Staff must understand how to instruct patients to receive appropriate medical care if a serious adverse reaction occurs such as difficulty breathing or signs of a stroke (including sudden difficulty speaking, numbness or weakness in the face, arms, or legs, difficulty walking, face drooping, severe headache, dizziness, or confusion) during or shortly after a procedure.
  • Discuss the benefits and risks of FDA-approved options for body contouring with patients.
  • Report to the FDA and, if applicable, the manufacturer if you become aware of a patient experiencing an adverse event associated with injectable silicone.

FDA Actions The FDA is monitoring reports of adverse events associated with the use of injectable silicone and other unapproved materials and will update the public if significant new information becomes available.

The FDA has investigated numerous criminal cases related to injectable silicone, which have resulted in successful prosecutions.

The FDA also is working with federal, state, and local law enforcement officials to inform them of these occurrences and to help prevent unlicensed providers from harming people through the injection of silicone and other unapproved materials.

Reporting Problems to the FDA Prompt reporting of adverse events can help the FDA to identify and better understand the risks associated with these products.

If you suspect or experience a problem with injectable silicone or a dermal filler, we encourage you to file a voluntary report through MedWatch, the FDA Safety Information and Adverse Event Reporting program. Health care personnel employed by facilities that are subject to the FDA’s user facility reporting requirements should follow the reporting procedures established by their facilities.

If you suspect you have been offered or have received injectable silicone from an unlicensed provider, we encourage you to report suspected criminal activity through the FDA’s website.

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