(KPLC/GRAY NEWS) — American Health Packaging is voluntarily recalling one lot of blood pressure medication to the consumer level due to the detection of trace amounts of an unexpected impurity, according to the FDA.
The impurity found is N-Nitrosodiethylamine, or NDEA; a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, and has been classified as a probable human carcinogen, FDA says.
Valsartan Tablets USP are used to control high blood pressure and for the treatment of heart failure, says the FDA. This product is distributed nationwide for use in hospital settings.
Here is the recalled product:
Valsartan Tablets USP 160 mg, 100 count Unit Dose Blisters, Carton NDC#: 60687-139-01, (Individual Dose NDC: 60687-139-11), 179791, Exp. Date: 3/31/2020
Patients who are prescribed Valsartan Tablets USP should continue taking their medication, as the risk of harm to the patient's health may be higher if the treatment is stopped immediately without any alternative treatment. No injuries have been reported.
Here are the five recalled medications:
1. Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide Tablets USP
2. Valsartan and Amlodipine and Valsartan tablets
3. Losartan Tablets USP 25 mg, 50 mg, and 100 mg
4. Losartan Potassium/Hydrochlorothiazide Combination Tablets
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