FDA hits Abbott FreeStyle Libre 3 recall with Class I tag
Abbott recalled the devices in July 2024 following incorrect readings by the CGM’s sensor.
![](https://www.medicaldevice-network.com/wp-content/uploads/sites/23/2024/09/shutterstock_2477302229.jpg)
Abbott recalled the devices in July 2024 following incorrect readings by the CGM’s sensor.
Representatives of the WHO and the IFRC called for international cooperation to tackle the current mpox outbreak.
The medical devices industry continues to be a hotbed of patent innovation. Activity is driven by increased need for homecare,...
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What is mpox and how big of a threat is it?