RF Safe reports that the U.S. FDA substantially revised its cellphone radiation webpages around January 15, 2026, removing or reducing prior language that broadly reassured the public about safety. The article argues the new framing more closely reflects the FDA’s statutory responsibilities under the Radiation Control for Health and Safety Act of 1968 (Public Law 90-602), emphasizing research, monitoring, and public information rather than definitive safety conclusions. It also links the change to a reported HHS announcement of a new study and portrays the update as a shift toward greater transparency, while noting some safety language may remain on the page.

This RF Safe commentary frames readers as part of a “resistance” movement seeking changes to U.S. wireless policy and RF exposure governance. It argues that current FCC RF exposure rules and related laws constrain local decision-making and rely on a “thermal-only” safety framework that the author says is outdated. The post cites a WHO-commissioned 2025 systematic review on RF-EMF and cancer in experimental animals as part of a broader WHO review effort, and advocates shifting indoor connectivity toward light-based technologies.

RF Safe argues that children’s everyday wireless exposure is primarily shaped by policy choices (laws, agency guidance, research mandates, and procurement practices) rather than by technology alone. The post promotes an “Act Now” hub that offers coordinated advocacy actions aimed at changing federal and local rules, increasing research and oversight, and shifting indoor connectivity toward alternatives such as Li‑Fi. It frames current governance as outdated and restrictive, particularly around local authority and federal agency accountability.

RF Safe promotes an “Act Now” hub intended to convert EMF safety concerns into policy and regulatory actions, emphasizing accountability and exposure reduction, especially for children. The page outlines five advocacy “levers,” including changing Section 704 of the Telecommunications Act, pressing the FCC to complete actions following a court remand, and restarting a federal electronic-product radiation program. It frames current RF oversight as outdated and insufficient for modern exposure patterns, and provides scripts to help supporters submit comments and demands into official records.

RF Safe founder John Coates outlines a 2026 advocacy plan focused on increasing enforcement of U.S. federal radiation-control law, pushing consumer technology toward Li‑Fi as a safer baseline for children, and demanding accountability from companies marketing wireless products to children. The post argues that current RF safety rules rely too heavily on “thermal-only” assumptions and that cumulative exposure from smartphones is a preventable risk. It also states RF Safe intends to pursue legal action to compel HHS to fulfill duties under the Radiation Control for Health & Safety Act (Public Law 90-602).

This RF Safe article defends the organization against accusations of bias, framing its EMF safety advocacy as rooted in founder John Coates’ personal tragedy and long-term efforts in product development, research synthesis, and policy reform. It claims RF Safe helped drive an FCC rule change related to antenna design and promotes various exposure-reduction accessories and training tools. The piece argues that non-thermal biological effects of RF/ELF fields are being overlooked by regulators and calls for policy changes such as revisiting Section 704 of the 1996 Telecom Act and shifting health oversight away from the FCC.

RF Safe publishes a commentary describing a public feud between Dr. Jack Kruse and RF Safe founder John Coates over how to address health concerns attributed to non-native electromagnetic fields (nnEMFs), especially regarding children. The piece portrays Kruse as emphasizing personal “light/circadian” biohacks and Coates as pushing technology and policy changes such as LiFi adoption and repealing/altering telecom-related legal constraints. It includes numerous claims about EMF-related harms and references to research (e.g., NTP/Ramazzini, a Henry Lai meta-analysis) but presents them within an advocacy narrative rather than as a balanced review.

An RF Safe commentary argues that the U.S. Department of Health and Human Services (HHS) is violating Public Law 90-602 by failing to continuously update radiation-safety standards, asserting that no formal revisions have occurred since the mid-1980s. The post links this alleged inaction to continued public exposure from wireless technologies and calls for renewed long-term research and stricter exposure limits. It also claims the National Toxicology Program (NTP) was shut down in 2024 and references a 2021 court decision criticizing FCC RF rules, urging congressional action and new legislation.

This RF Safe article argues that U.S. radiofrequency (RF) exposure policy is outdated, emphasizing that FCC limits adopted in 1996 are based on preventing tissue heating and do not address alleged non-thermal biological effects. It claims responsibility for protecting public health from electronic product radiation was effectively ceded from health agencies to the FCC, and that Section 704 of the Telecommunications Act limits local governments from opposing wireless infrastructure on health grounds if FCC limits are met. The piece cites epidemiology, cell studies, and animal studies (notably the U.S. National Toxicology Program and the Ramazzini Institute) to argue that evidence has accumulated and regulation should be updated, but it presents these points in an advocacy framing rather than as a balanced review.

RF Safe argues that an FDA-authorized therapeutic radiofrequency device (TheraBionic P1) demonstrates biologically meaningful “non-thermal” RF effects, and contrasts this with consumer wireless regulation that it says is based primarily on heating (SAR) limits set in 1996. The post frames this as a regulatory and legal gap, citing the Radiation Control for Health and Safety Act and Telecommunications Act Section 704 as factors limiting local and public-health oversight. It also references several epidemiology and animal studies (e.g., Interphone, Hardell, CERENAT, IARC 2011 classification, and the U.S. NTP rodent studies) to support the claim that non-thermal effects and health risks warrant stronger scrutiny, though the article’s presentation is advocacy-oriented.

RF Safe argues that HHS is not complying with Public Law 90-602’s requirements to run an electronic product radiation control program, support research, and make results publicly available. The post claims the National Toxicology Program (NTP) RF bioeffects work was halted in 2024 and has not restarted, and calls for immediate resumption with open data and a public timetable. It also presents a mechanistic narrative and cites various animal and cell-study findings as support for potential non-thermal RF biological effects, alongside policy recommendations such as LiFi-first guidance for schools and updated standards that account for signal timing characteristics.