Safety Alert Due To Marketing Of Unapproved Stem Cell And Exosome Products
, The National Agency for Food and Drug Administration and Control has been informed by US FDA of illegal “stem cell” products offering exosome products to patients. They deceive patients with unsubstantiated claims about the potential for these products to prevent, treat or cure various diseases or conditions. There are currently no FDA-approved exosome products. Exosomes […]
GL Holdings Issues Voluntary Worldwide Recall Of Green Lumber Products Due To Presence Of Undeclared Tadalafil
, The National Agency For Food And Drug Administration And Control Has Been Notified By The US Food And Drug Administration That GL Holdings Is Voluntarily Recalling Six Lots Of Green Lumber 2-, 4-, And 10-Capsule Packages Purchased On Or Before August 10, 2019 To The Consumer Level. This Recall Was Due To FDA’s Analysis […]
SUBJECT: Recall Of Ranitidine Tablets USP 150mg And 300mg By Glenmark Pharmaceuticals
, The National Agency for Food and Drug Administration and Control has been notified by the United States Food and Drug Administration that GLENMARK PHARMACEUTICALS is voluntarily recalling Ranitidine tablets USP 150mg and 300mg due to possible presence of N-nitrosodimethylamine (NDMA) impurity. Ranitidine is a drug that belongs to the group called Histamine-2 blockers used […]
Recall Of Drugs, Dietary Supplements And Devices By Basic Reset And Biogenyx
, The National Agency for Food and Drug Administration and Control has been informed by the U.S Food and Drug Administration (FDA) of a recall of 25 drugs by basic reset and biogenyx of Hendersonville, Tennessee due to consent decree for federal violations and unlawfully distribution of dietary supplements that are adulterated and misbranded. Basic […]
