Silicone Safety and Information Act
Official title: To amend the Federal Food, Drug, and Cosmetic Act to require that physicians who perform silicone gel implants provide certain information to patients.
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Referred to the Subcommittee on Health and the Environment.
Silicone Safety and Information Act - Amends the Federal Food, Drug, and Cosmetic Act to require a physician performing a silicone gel implant to provide the patient in advance with a summary prepared by the Secretary of Health and Human Services respecting the associated advantages, disadvantages, and risks. Directs the Secretary to provide such a summary to physicians. Sets forth a civil monetary penalty for violations by physicians.
- Introduced in House Formatted Text
Cite this page
U.S. Congress. (2026). H.R. 1422: Silicone Safety and Information Act. 102nd Congress. Open America. https://openamerica.io/bill/102-HR-1422/
"H.R. 1422: Silicone Safety and Information Act." 102nd Congress, 2026, Open America, https://openamerica.io/bill/102-HR-1422/.
H.R. 1422, 102nd Cong. (2026), https://openamerica.io/bill/102-HR-1422/.
[H.R. 1422: Silicone Safety and Information Act](https://openamerica.io/bill/102-HR-1422/)