Over 580,000 Blood Pressure Medication Bottles Recalled, FDA Reports

Recall of Blood Pressure Medication

Over 580,000 bottles of blood pressure medication have been recalled by the FDA due to the presence of a potential carcinogenic impurity.

The recall affects certain lots of prazosin hydrochloride capsules, specifically 1mg, 2mg, and 5mg bottles, which can be identified by lot number and expiration date.

No one wants to trade high blood pressure for a potentially cancer-causing chemical.

It is essential to consult a physician before stopping any medication, even if the bottles are affected by the recall.

Affected bottles can be identified using the lot number and expiration date outlined in the FDA report.

Author's summary: FDA recalls blood pressure medication.

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Prevention Prevention — 2025-10-31

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