(KPLC)
- 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:
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 US
5. See the current recall HERE.
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Friday, March 8, 2019
Fifth hypertension medication recalled in two weeks
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