- The US Food and Drug Administration (USFDA) said that Aurobindo Pharma USA is recalling 9,504 bottles of medicine used to treat high blood pressure from the US market.
- According to the USFDA, the lot was recalled because of “CGMP violations from current good manufacturing standards.”
- The recalled Quinapril and Hydrochlorothiazide tablets were marketed in the US by Aurobindo Pharma USA and were made in India.