medical device recalls

Medical device recalls occur when a product is found to have safety issues or defects that could harm patients. This can happen before or after the device is used. The recall may result from reports of malfunction, design flaws, or failure to meet health standards. The manufacturer, often under the guidance of regulatory agencies like the FDA, may inform the public, offer repairs, replacements, or refunds, and recommend that users stop using the device. Recalls are crucial for protecting patient safety and ensuring that medical devices function as intended.