The Food and Drug Administration posted information on its website listing the blood pressure medications recalled for containing carcinogens. Here's what to watch out for.
Macleods Pharmaceuticals Limited is recalling 32 lots of the popular blood pressure drug, losartan after discovering trace amounts of probable carcinogens.
The recalled losartan and potassium / hydrochlorothiazide combination tablets contained small amounts of N-nitrosodiethylamine, or NDEA, according to a company notice posted to the Food and Drug Administration's website Wednesday.
Cancer in a few patients following long-term use of the product cannot be ruled out, "the recall notice states.
The active drug ingredient was manufactured at Hetero Labs Limited in India, one of the overseas drug factories linked to repeated blood medication recalls since last July
Macleods also recalled one lot of the losartan combination drug in February for the same reason. The company said in the statement that it has not received any reports of adverse effects. " MacBook Pro recall: Apple voluntarily recalling batteries on MacBook Pro notebooks due to safety risk
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Health care professionals advise patients with consulting their doctors or pharmacists before discontinuing one of the recalled blood pressure medicines or finding an alternative treatment. medication
Consumers with medical questions or to report and adverse event can contact Macleods at 855-926-3384 from 8 am to 5 p.m. EST.
For questions about returning the product, contact Qualanex via email at email@example.com or call 888-280-2046 from 7 a.m. to 4 p.m. CST weekdays.
Was your medicine recalled?
Here are the doses, lot numbers and expiration dates of the recalled medicine: Losartan Potassium Tablets 50 mg:
- BL1711A, BLl710A, November 2019
Losartan Potassium and Hydrochlorothiazide Tablets 50 mg / 12.5 mg:
- BLK719A, BLK724A, BLK724A, September 2019 BLK725A, BLK726A, October 2019
- BLK804A, BLK806A, January 2020
- BLK825A , BLK826A, October 2021