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FDA Warns Against Using Smartwatches For Blood Glucose Monitoring

Signage is seen outside of FDA headquarters in White Oak, Maryland

The Food and Drug Administration (FDA) has issued a warning to consumers regarding the use of smartwatches to measure blood glucose levels. The FDA cautions that these devices may not provide accurate or reliable results, potentially leading to serious health risks.

Smartwatches equipped with sensors claim to offer convenient and non-invasive ways to monitor blood glucose levels. However, the FDA emphasizes that these devices have not undergone rigorous testing to ensure their accuracy in measuring such a critical health parameter.

According to the FDA, inaccurate blood glucose readings could result in incorrect treatment decisions for individuals with diabetes. This could lead to either dangerously high or low blood sugar levels, posing significant health hazards.

The FDA advises consumers to rely on traditional, FDA-approved methods for monitoring blood glucose levels, such as fingerstick tests or continuous glucose monitors. These established methods have been scientifically validated and are considered safe and effective for managing diabetes.

Health experts recommend consulting healthcare professionals before using any new technology or device for monitoring health conditions. It is crucial to prioritize accuracy and reliability when it comes to managing chronic conditions like diabetes.

In response to the FDA warning, manufacturers of smartwatches with blood glucose monitoring features are urged to conduct thorough testing and seek FDA approval to ensure the safety and efficacy of their products.

Consumers are encouraged to stay informed about the latest updates and advisories from regulatory authorities like the FDA to make informed decisions about their health and well-being.

As technology continues to advance in the healthcare sector, ensuring the accuracy and reliability of health monitoring devices remains paramount to safeguarding public health.

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