Monitoraggio anticorpi monoclonali per COVID-19: pubblicato l'ottavo report
Italiano
The SARS-CoV-2 Antigen Rapid Test Kit and Leccurate SARS-CoV-2 Antibody Rapid Test Kit (Colloidal Gold Immunochromatography) have a likely risk of false results
There is likely a high risk of false results using these tests. The tests are not FDA authorized, cleared, or approved.
Bezel posts on the Alaris Infusion Pump Module 8100 are critical to pump function. Step-Har repair bezel posts may crack or separate.
Dash Xclusive is voluntarily recalling all lots of Imperia Elita Vitaccino Coffee to the consumer level. FDA analysis has found the product to contain undeclared sibutramine and fluoxetine.
Read more on the domestic supply of new respirators, including N95s and other FFRs, elastomeric respirators, powered air-purifying respirators (PAPRs)
FDA is restricting the use of the liver disease medicine Ocaliva (obeticholic acid) in patients having primary biliary cholangitis with advanced cirrhosis of the liver because some patients with cirrhosis who took Ocaliva, especially those with evidence of advanced cirrhosis, developed liver failure
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