The FDA has introduced a nationwide recall of greater than 580,000 bottles of blood strain medicine after exams discovered traces of a cancer-causing chemical in sure batches. The affected drug, Prazosin Hydrochloride, was distributed in 1 mg, 2 mg, and 5 mg capsule varieties by Teva Prescription drugs and Amerisource Well being Providers.
Well being specialists are urging sufferers to not cease taking their medicine abruptly, as uncontrolled blood strain could be harmful. As an alternative, customers ought to test the lot quantity on their prescription bottles and speak to their physician or pharmacist if their medicine seems on the recall listing.
The FDA says the problem includes nitrosamine impurities, a category of compounds linked to an elevated threat of most cancers with long-term publicity. Right here’s every little thing to know concerning the blood strain medicine recall, the medication affected, and what steps sufferers ought to take subsequent.
Which Blood Stress Drugs Have been Recalled?
The recall impacts Prazosin Hydrochloride capsules in 1 mg, 2 mg, and 5 mg strengths, distributed nationwide beneath the Teva Prescription drugs label. Greater than 580,000 bottles have been affected, with expiration dates starting from April 2026 by means of September 2027. The drug, usually used to deal with hypertension and post-traumatic stress dysfunction (PTSD)-related signs, has been pulled from cabinets on account of contamination considerations.
Sufferers can confirm if their prescription is a part of the recall by checking the lot numbers listed on the FDA’s official recall discover. If a match is discovered, the FDA advises contacting a healthcare supplier earlier than making any medicine adjustments.
Why Was This Blood Stress Remedy Recalled?
In response to the FDA, the medicine contained “above acceptable consumption limits” of a nitrosamine compound known as N-nitroso Prazosin impurity C—a part of a category of chemical substances linked to an elevated threat of most cancers. The recall was formally categorized as Class II, which means the potential for severe hurt is taken into account distant however nonetheless medically regarding.
Whereas the FDA’s Class II recall classification means most individuals are unlikely to expertise extreme results, the company warns that “non permanent or medically reversible hostile well being penalties” may happen. Teva famous that different remedies for hypertension stay broadly accessible and reaffirmed its dedication to high quality management, stating, “There are a lot of different remedies accessible to sufferers.”
“Teva prioritizes affected person security and product high quality at each stage of a medication’s lifecycle.”
The compound, N-nitroso Prazosin impurity C, can type throughout the manufacturing or storage course of.
