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Search resuls for: "Prestige Biotech"


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CNN —Consumers shouldn’t use certain tests manufactured by Universal Meditech Inc., the US Food and Drug Administration warned Friday, including those that test for pregnancy, ovulation and urinary tract infections. “UMI has notified the FDA that it has stopped all operations and is no longer providing support for its tests,” the agency said. “The FDA is not able to confirm the performance of UMI’s tests, raising concerns that the tests may not be safe and effective.”The California-based company has recalled undistributed tests but not those that have already been distributed to consumers. Consumers are advised not to purchase or use the following Universal Meditech tests but rather to throw them away:One Step Pregnancy TestDiagnosUS One Step Ovulation TestHealthyWiser UriTest 10 Parameter Reagent Test Strips for UrinalysisHealthyWiser UriTest UTI Test StripsHealthyWiser KetoFast Ketone Test StripsHealthyWiser pH-Aware pH Test StripsTo Life hCG Pregnancy Urine TestAm I Pregnant Pregnancy Midstream TestDeTec hCG Pregnancy Urine TestPrestiBio Pregnancy StripsPrestiBio Rapid Detection Pregnancy Test MidstreamPrestiBio Ovulation StripsPrestiBio Urinalysis Test Strip 10 ParametersPrestiBio Ketone Test StripsPrestiBio Breast Milk Alcohol Test StripsThe tests may have been distributed under brand names such as AC&C, HealthyWiser, Home Health US and Prestige Biotech. Consumers may report problems with devices or tests to the FDA through its MedWatch program.
Persons: UMI Organizations: CNN, Universal Meditech Inc, US Food and Drug Administration, FDA, Universal, Home Health, Prestige Biotech Locations: The California
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