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The U.S. Food and Drug Administration says more than 580,000 bottles of prazosin hydrochloride have been voluntarily recalled nationwide over possible nitrosamine impurities considered potentially cancer causing. New Jersey-based Teva Pharmaceuticals USA and distributor Amerisource Health Services initiated the recall of multiple capsule strengths earlier this month. The FDA assigned the affected lots a Class II risk, noting that prazosin relaxes blood vessels to lower blood pressure and is sometimes used for PTSD-related nightmares and sleep disturbances.

Prepared by Olivia Bennett and reviewed by editorial team.