The Dexcom Continuous Glucose Monitor Receiver Recall: What You Need to Do to Stay Safe

Dexcom, a leading manufacturer of continuous glucose monitoring (CGM) systems, has issued a recall for certain models of its CGM receivers. This is a Class I recall, the most serious type, indicating a reasonable probability of serious injury or death if the device is used. The recall affects approximately 206,000 Dexcom G4 and G5 CGM receivers, with 56 reported cases of serious injury. The issue lies in the receiver's inability to reliably display accurate glucose readings, potentially leading to incorrect treatment decisions. Dexcom has advised users to immediately stop using the affected receivers and contact the company for a free replacement. Patients are encouraged to use the Dexcom G6 mobile app or a compatible smart device as an alternative until a new receiver is obtained. This recall highlights the importance of staying informed about medical device safety and following the manufacturer's guidance to ensure the continued safe and effective use of CGM systems. Patients should consult their healthcare providers for further assistance and guidance during this recall process.