Philips Undertakes Proactive Correction of Cardiac Monitoring Software, Ensures Continuing Patient Safety
Amsterdam, Netherlands — Philips, a global leader in health technology, has taken swift action to address a software configuration issue in its Mobile Cardiac Outpatient Telemetry (MCOT) devices, ensuring no products are recalled or removed from the market. Customers are advised to adhere to the guidelines provided in the Urgent Medical Device Correction notice they received, which includes instructions for rereading potentially affected ECG data. This proactive approach by Philips follows the discovery of the …