FDA: Risk of False Results With HSV-2 Serologic Tests for Genital Herpes
The FDA is advising health care providers and clinical laboratory staff of the risk for false positive results with HSV-2 serological tests.
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The FDA is advising health care providers and clinical laboratory staff of the risk for false positive results with HSV-2 serological tests.
The FDA is warning health care providers about the risk of invasive disease in preterm infants administered probiotics.
The FDA is requiring updated warnings for prescription stimulants to ensure the safe use of these medications.
The FDA announced the recall of certain Philips Respironics CPAP and BiPAP masks due to a safety concern involving magnets.
The magnetic headgear clips are used to attach the headgear straps to the masks, which is a method that is commonly used in the sleep therapy devices industry.