Hologic has created the following letter regarding recall. URGENT: MEDICAL DEVICE RECALL BioZorb® 3D Bioabsorbable Marker Dear Valued Hologic Customer, Hologic Inc.,…
Browsing: Regulatory
The FDA has new recommendations for how to prevent the risk of damage caused by electronic interference with wearable devices…
In observance of Breast Cancer Awareness Month, the U.S. Food and Drug Administration’s (FDA) Center for Devices and Radiological Health…
In recognition of World Patient Safety Day, the Biden-Harris Administration is announcing actions to address patient and workforce safety in…
Key insights and patient safety commitments follow D.C. summit The White House Office of Science and Technology Policy (OSTP) convened…
Today, the final rule to update the mammography regulations that were issued under the Mammography Quality Standards Act of 1992…
The Architectural and Transportation Barriers Compliance Board has issued a final rule to remove the sunset provisions in the board’s existing accessibility…
To obtain feedback about ways to help ensure that all patients have timely access to safe, effective, and high-quality medical…
The U.S. Food and Drug Administration (FDA) updated its Recognized Consensus Standards database. This latest update, known as “List 62,”…
The FDA provides annual and quarterly reports on its progress towards meeting performance goals and commitments set under MDUFMA to…
