Dec 17, 2020 | News, Regulatory
Following the close of the market on Tuesday, Penumbra announced the U.S. Food and Drug Administration (FDA) advised recall of their catheter device resulting from 14 reported patient deaths, among other patient hemorrhages,... 
Oct 9, 2020 | News, Regulatory
Marksans Pharma and Sun Biophamrmaceuticals Industries are facilitating recalls through the FDA of their drug Metaformin as a result of high NDMA (N-nitrosodimethylamine) it contains. The FDA released a comprehensive list of Metaformin products being recalled. It is...
