What is the name of the federal program that allows voluntary reporting of device-related problems?

MedWatch is the federal program designed to facilitate the voluntary reporting of device-related problems, as well as other product safety issues. It serves as a mechanism for healthcare professionals, patients, and manufacturers to report adverse events, product quality problems, and medication errors associated with medical devices, drugs, and dietary supplements. By providing this voluntary reporting system, MedWatch enhances patient safety by actively collecting information that can be analyzed to identify potential risks and address concerns in the medical field.

This program is essential for the ongoing monitoring of medical devices after they have been approved for use, as it helps to ensure that issues can be identified and managed promptly. In contrast, the other options listed do not represent official federal programs designed specifically for this purpose.