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The 2020 recall came eight years after Fitbit recalled its Fitbit Force activity-tracking wristband after the company received roughly 9,900 reports of the wristband irritating skin and 250 ...
In 2014, Fitbit halted sales and recalled a million of its Fitbit Force smartwatches over reports related to skin irritation. Fitbit is not the only company to face claims over product hazardousness.
Fitbit Alta HR fitness tracker wristband showing heart rate monitor display. The Fitbit Alta [41] was released in February 2016. The wristband offers a full OLED screen that can be tapped for reminders, a clock and smartphone notifications. While not a touch screen, it is interacted with by tapping the band, similar to previous models.
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.
(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 ...
In 2014, Flextronics was named as the manufacturer of the Fitbit Force by the US Consumer Product Safety Commission in the context of a complete recall of the product due to rashes developing on the wrists of its users. [11] In July 2015 the company announced it changed the company name from Flextronics to Flex. [12]
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 ...
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.