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Universal Meditech Inc. Expands Nationwide Recall to All Products Manufactured between March 2021 and November 2022

Universal Meditech Inc. initiated a nationwide recall of products it manufactured between March 2021 and November 2022. The recall is due to the reasons that: i. The company is going out of business, hence would not be able to continue fulfilling any post-market responsibilities of these distributed
New Jersey United States New York Healthywiser Uritest Las Vegas Healthywiser Ketofast
Source: fda.gov

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Universal Meditech Inc. Issues Nationwide Recall of All Products Manufactured Between March 2021 and November 2022

On July 1, 2023, Universal Meditech Inc. initiated a nationwide recall of products it manufactured between March 2021 and November 2022. The recall is due to the reasons that: i.The company is going out of business, hence would not be able to continue fulfilling any post-market responsibilities of
New Jersey United States New York Healthywiser Uritest Healthywiser Ketofast Meditech Inc
Source: fda.gov

FDA Issues Update on Abbott Trifecta Valves: Potential Risk of Early Structural Valve Deterioration

The U.S. Food and Drug Administration (FDA) is providing an update to the February 27, 2023 Letter to Health Care Providers about the potential risk of early structural valve deterioration (SVD) with Abbott Trifecta valves, including the Trifecta Valve and Trifecta Valve with Glide Technology (GT)
United States Letter To Health Care Providers Technology Trifecta Drug Administration Health Care Providers Abbott Trifecta

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