DexCom Faces Class Action Lawsuit Over Alleged False Statements on Glucose Monitor Safety

Reuters12-08

DexCom Faces Class Action Lawsuit Over Alleged False Statements on Glucose Monitor Safety

A class action lawsuit has been filed against DexCom Inc. on behalf of investors who suffered losses between January 8, 2024, and September 17, 2025, due to alleged securities fraud. The complaint alleges that DexCom made unauthorized material design changes to its glucose monitoring products, the G6 and G7, without FDA approval. These changes reportedly made the devices less reliable and posed significant health risks to users. It is further alleged that DexCom overstated the reliability, accuracy, and functionality of the G7, downplayed the severity of the issues, and misrepresented the company's exposure to regulatory and financial risks. The ongoing litigation seeks to recover damages for shareholders affected by these alleged misstatements.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. DexCom Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1115400) on December 08, 2025, and is solely responsible for the information contained therein.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

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The complaint alleges that DexCom made unauthorized material design changes to its glucose monitoring products, the G6 and G7, without FDA approval. These changes reportedly made the devices less reliable and posed significant health risks to users. It is further alleged that DexCom overstated the reliability, accuracy, and functionality of the G7, downplayed the severity of the issues, and misrepresented the company's exposure to regulatory and financial risks. The ongoing litigation seeks to recover damages for shareholders affected by these alleged misstatements.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. DexCom Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. 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