Voluntary recall for blood pressure medication due to cancer causing ingredient

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The International Agency for Research on Cancer has identified it as a probable human carcinogen.

Losartan Potassium Hydrochlorothiazide Tablets, USP are indicated for the treatment of hypertension. FDA said they found some contamination: N-nitrosodiethylamine (NDEA) in some of these drugs and that's they have recalled them to prevent any further consumption of these contaminated drugs. It may be used alone or in combination with other antihypertensive agents.

This is the third blood pressure medication to face recall as of late. Now, if the lot carries the number JB8912, then the patient has with him or she recalled pills. They should quarantine any remain qualities and return them to the identified reverse distributor.

For any questions place contact Sandoz at 1-800-525-8747. Patients who are on Losartan Potassium Hydrochlorothiazide should continue taking their medication, as the risk of harm to a patient's health may be higher if the treatment is stopped immediately without any alternative treatment. The online reporting form can be completed online at www.fda.gov/medwatch/report.htm. However, it said, no issues have been reported concerning the affected tablets.

The FDA recently recalled blood pressure drug irbesartan for the same defect. FDA has also published a complete list of those effective drugs which they have recalled and most of these drugs used to sold in 75 mg, 150 mg, and 300 mg doses.

The latest recall impacts less than 1 percent of the total losartan drug products in the USA market, according to the FDA.

Sandoz has recalled a blood pressure medication because of an impurity that could cause a cancer risk.

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