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FDA announces another blood pressure medication recall

By Natalie Dreier, Cox Media Group National Content Desk

A single lot of hydrochlorthiazide tablets have been recalled due to a mislabeling issue.

By Natalie Dreier, Cox Media Group National Content Desk

The Food and Drug Administration has announced another blood pressure medication is under a recall.

This time, it is a specific lot made by Accord and the recall is due to the mislabeling of the medication.

The bottle, according to the FDA, is labeled as hydrochlorthiazide tablets, but the bottle in reality contains spronolactone tablets.

Hydrochlorothiazide tablets are used to manage hypertension.

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Spironolactone is used to manage primary hyperaldosteronism and edematous (or swelling) conditions for patients with congestive heart failure, cirrhosis of the liver, nephrotic syndrome, essential hypertension or hypokalemia, according to the FDA.

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Accord’s hydrochlorothiazide tablets USP 12.5mg, are light orange with an H on one side and the number 1 on the other.

The recall is specific to the individual lot number PW05264.

The company was alerted to the problem after a pharmacy reported it, the FDA said.

If someone takes a spironolactone tablet instead of a hydrochlorothiazide one, they could have increased potassium levels that could impact their health or even lead to life-threatening situations, according to the FDA.

Consumers with questions can contact Accord at 1-855-869-1081 or via email at rxrecalls @inmar.com.

If you have taken the mislabeled medication, you can contact the FDA at this link.

Earlier this year, the FDA announced, and eventually expanded, the recall of

Torrent Pharmaceuticals Limited's valsartan/amlodipine/hydrochlorothiazide tablets after trace amounts of N-nitrosodimethylamine (NDMA) were found in one of the drug's active ingredients.

 

Cox Media Group

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