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“I have been prosecuting serious injury and wrongful death cases against trucking companies, auto makers and tire manufacturers for more than 30 years. Our firm maintains this blog to share information and insight on transportation safety issues that continue to arise on our nation’s highways and roads.”

Dexcom Recalls Defective CGM Glucose System Receivers Due to Serious Adverse Events


Dexcom has provided an update on its ongoing recall of continuous glucose monitoring (CGM) receivers, which the FDA previously classified as Class I—the agency’s most serious recall category due to the risk of severe injury or death.

The recall affects components of the Dexcom One, One+, G6, and G7 systems, including receivers used to alert patients when glucose levels are dangerously high or low. A defect involving the receiver’s speaker, attributed to faulty foam or assembly issues, may cause it to fail to sound alarms during critical glucose events. The FDA cited a nonconforming component as the root cause.

Dexcom has received at least 112 complaints tied to the issue, with 56 reports of serious adverse events such as seizures, unconsciousness, and other symptoms possibly linked to missed alerts.

Contact The Ammons Law Firm for Legal Help Involving Defective Products

Contact The Ammons Law Firm today for a free consultation to discuss your case and learn more about your legal options. You may be entitled to compensation for medical expenses, lost wages, pain and suffering, and other damages caused by this defective product.

 

 

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