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OneTouch Ultra blood glucose meters provide blood glucose test results in five seconds. The device offers alternative test site options, as well as various memory and flagging features. The results are displayed as plasma values. It is used to measure glucose levels for both hypoglycemia and hyperglycemia in children and adults. [2][3]
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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 ...
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]
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 ...
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 ...
Abiomed, Inc. is a medical device technology company that operates as a stand-alone business within Johnson & Johnson's MedTech Segment. [2] Abiomed develops and manufactures temporary external and implantable mechanical circulatory support devices. The company is headquartered in Danvers, Massachusetts with additional offices in Woburn ...
The California-based medical device maker started the recall process on Nov. 20 and has recalled over 20 mill US FDA identifies recall of ResMed's respiratory devices as most serious Skip to main ...