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Google-owned Fitbit has recalled 1 million of its Ionic smartwatches after dozens of users reported burn injuries because the battery overheated. The fitness gadget maker says consumers who bought ...
(Reuters) - Google-owned Fitbit has recalled more than a million of its Ionic smartwatches following reports that overheating batteries had caused burn injuries, the U.S Consumer Product Safety ...
Google is being sued by two women over its Fitbit smartwatches, court filings show. The fitness firm previously 1.7 million of its Ionic Smartwatch over safety concerns.
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.
An FDA warning letter is an official message from the United States Food and Drug Administration (FDA) to a manufacturer or other organization that has violated some rule in a federally regulated activity.
The Fitbit Charge 3, a wristband health and fitness tracker introduced in October 2018, was the first device to feature an oxygen saturation (SPO2) sensor; however, as of January 2019, it was non-functional and Fitbit did not provide an implementation timeline. [44] The Fitbit Charge 3 comes with two different-sized bands: small and large.
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Fitbit Surge. Announced in October 2014, the Surge was a smart watch and an activity tracker. It features a heart-rate monitor and the ability to track pace, distance, and elevation using the GPS on the device. The Surge also can send alerts of text and incoming calls from a connected smartphone.