The FDA Issued a Recall on Bladder Medication Nationwide

The FDA Issued a Recall on Bladder Medication Nationwide

Open the article to view the coverage from EatingWell

Recall ordered for batch of hypertension drugs

The Food and Drug Administration (FDA) yesterday ordered a recall of a batch of hypertension drug, consisting of 87,360 tablets.The FDA said it received notification of a defective drug product — Beniel F.C. Tablets 8mg, batch code 2KA31 — manufactured by Synmosa Biopharma Corp. The batch was regist

Common Blood Pressure Drug Recalled Nationwide, FDA Says

Novartis Pharmaceuticals Corporation recalled some heart failure and high blood pressure medication due to potency issues, according to the Food and Drug Administration’s website. The recall affects one lot of Diovan, Novartis’ valsartan brand, according to a report issued last week. The lot includes 160-milligram tablets in 90-count bottles, with the lot number AV5913C, and an expiration date of June 2027. The drug is prescription-only and manu…

TFDA orders recall of over 87,000 antihypertensive tablets

Taipei, Aug. 12 (CNA) The Taiwan Food and Drug Administration (TFDA) has ordered the recall of 87,360 tablets of the antihypertensive drug Beniel F.C. Tablets 8 mg manufactured by Synmosa Biopharma Corp. over concerns that the medication may not work as intended, the agency said Wednesday.