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Wednesday, 12 November, 2025
HomeNews UpdateFDA recalls 600 000 bottles of BP drug over cancer risk

FDA recalls 600 000 bottles of BP drug over cancer risk

The FDA said drugmakers have recalled more than 580 000 bottles of a blood pressure medication over concerns it may include a cancer-causing chemical, with Teva Pharmaceuticals USA and distributor Amerisource Health Services issuing voluntary recalls this month for the containers of various strengths of prazosine capsules.

Known as prazosin hydrochloride, the capsules come in 1 mg, 2 mg and 5 mg doses, reports CBS News. It helps relax blood vessels to facilitate blood flow and is sometimes prescribed for nightmares and other sleep disturbances caused by post-traumatic stress disorder.

Teva Pharmaceuticals did not immediately respond to a request for comment.

In its recall orders posted on its website, the FDA said it has classified the affected lots as a Class II risk because some may have nitrosamine impurities that are considered potentially carcinogenic.

The chemicals can form when a drug is manufactured or stored, according to the agency.

 

CBS News article – 580,000 bottles of a blood pressure drug recalled over cancer risk, FDA says (Open access)

 

See more from MedicalBrief archives:

 

FDA carcinogen-related recalls could cause shortages of hypertension drug

 

FDA issues voluntary recall of generic blood pressure drug

 

FDA recalls anxiety drug after dangerous labelling error

 

FDA warning after recall of contraceptive pill batches

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