What should manufacturers do in response to a report of adverse effects not included in a device package insert?

When manufacturers receive a report of adverse effects that are not included in the device package insert, it is crucial for them to report the incident to the FDA. This is a key regulatory requirement aimed at ensuring patient safety and maintaining the integrity of medical products in the market. Reporting such incidents allows the FDA to monitor safety trends, assess risks associated with medical devices, and take appropriate action if necessary.

By reporting the adverse effects, manufacturers contribute to the overall vigilance system that helps identify potential safety issues that may not be apparent in clinical trials or previous usage. The FDA relies on these reports to determine if further investigation or corrective actions are needed, which could include label changes, product recalls, or additional safety studies.

Taking immediate action by reporting enhances the responsiveness of the regulatory system to potential threats to patient safety and reinforces the manufacturer’s commitment to compliance and proactive risk management.