What a Class I Recall Means for a Medical Device
Learn why FDA's highest-risk device recall may require repair, monitoring, reprogramming or removal.
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How the FDA Approves a New Drug
Follow a new drug from laboratory studies through clinical trials, FDA review and possible accelerated approval.
Read more →Massachusetts Law Gives Physicians Discretion Over Abortions After 24 Weeks
Massachusetts Governor Maura Healey signed H.5595, An Act Prioritizing Patient Access to Care, on August 10, 2026, eliminating the state's four-part framework governing abortions...
Boston.com
Read more →FDA Issues Class I Recalls for Resmed Astral Ventilators and Abiomed Introducer Kits
The U.S. Food and Drug Administration identified Class I recalls — its most serious category — for certain Astral ventilators made by Resmed and...
American Hospital Association / U.S. Food and Drug Administration
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