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The US Food and Drug Administration issued a warning Wednesday about the risks of using smartwatches and smart rings that claim to measure blood glucose levels without piercing the skin.
The agency added it has not authorized, cleared, or approved any smartwatch or smart ring that is intended to measure or estimate blood glucose values on its own. FDA warns consumers over use of ...
Nearly a week after Lupin Pharmaceuticals announced a voluntary recall of two types of blood pressure medications, the company continues to see its stock price slide (though the hit could have ...
[71] [72] On March 2, 2022, Fitbit issued a voluntary recall of 1.7 million Ionic smartwatches, citing overheating issues with the battery posing a burn hazard. [73] [74] At the time of the recall, there were 78 reports of skin burns in the United States and 40 internationally (and 115 reports of overheating in the US and 59 internationally).
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
Wearable technology is any technology that is designed to be used while worn.Common types of wearable technology include smartwatches and smartglasses.Wearable electronic devices are often close to or on the surface of the skin, where they detect, analyze, and transmit information such as vital signs, and/or ambient data and which allow in some cases immediate biofeedback to the wearer.