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The OneTouch Ultra 2 Meter is being used by a diabetic patient. OneTouch Ultra is a blood glucose monitoring device for people with diabetes that is manufactured by Johnson & Johnson . [ 1 ] It is the foundation product for LifeScan's OneTouch Ultra family of blood glucose monitoring systems .
Launched in March 2018, the Fitbit Ace is essentially a version of the Alta for children aged 8 and above. In March 2019, the Fitbit Ace 2 for kids aged 6 to 12 was announced. In March 2021, the Fitbit Ace 3 was released, adding a curvier appearance, also for ages 6–12. [2][3] In July 2024, Fitbit has announced the new Fitbit Ace LTE.
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LifeScan was established in 1981. [3] It was acquired by Johnson & Johnson (J&J) in 1986, [2][4] and in June 2018, J&J agreed to sell LifeScan to Platinum Equity as part of its strategic exit from the diabetes device market, accepting an offer originally tendered in March 2018. [1] The divestiture completed in October 2018. [1][5]
Johnson & Johnson's LifeScan unit is recalling all of its OneTouch Verio IQ blood glucose meters in the U.S. At extremely high blood glucose of 1024 mg/dL or higher, the machine just shuts off ...
The Pipeline Flex Devices include a guidewire-based delivery system used to place the implant inside the patient. The FDA says that fractured pieces could be Medtronic Recalls Pipeline Flex ...
Recall information. FDA develops a strategy for each individual recall that sets forth how extensively it will check on a company's performance in recalling the product in question. For a Class I recall, for example, FDA would check to make sure that each defective product has been recalled or reconditioned. In contrast, for a Class III recall ...
Use of the device may cause serious injury, including blood loss, artery tears, unstable blood pressure, prevention of blood flow to the heart, or death, according to the FDA.