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Drug Recalls News

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Teva Pharmaceuticals USA is recalling several lots of desmopressin acetate tablets over concerns product bottles may not contain desiccants. The recall is included in the February 12, 2020, US Food and Drug Administration (FDA) Enforcement Report.  The recall affects the following products: …
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Ascend Laboratories is pulling 4728 bottles of minocycline hydrochloride extended-release tablets because samples failed to meet dissolution specifications during routine testing, according to the February 12, 2020, US Food and Drug Administration (FDA) Enforcement Report.  The recall affects 30-…
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Nearly 30,000 bottles of 10-mg atorvastatin calcium tablets are being recalled by Graviti Pharmaceuticals after a customer reported finding a 20-mg tablet in a bottle, according to the  February 12, 2020, US Food and Drug Administration (FDA) Enforcement Report.  The recall includes 90-count…
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Mylan Pharmaceuticals Inc. is recalling more than 48,000 bottles of nizatidine capsules after trace amounts of the probable human carcinogen N-Nitrosodimethylamine (NDMA) were detected in the medication, according to the January 29, 2020, US Food and Drug Administration (FDA) Enforcement Report.…
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New ranitidine recalls prompted by suspected product contamination with the probable human carcinogen N-Nitrosodimethylamine (NDMA) have been announced by four firms. The latest recalls were included in the January 29, 2020, US Food and Drug Administration (FDA) Enforcement Report.  On December 11…
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Sun Pharmaceutical Industries Inc. has recalled multiple drugs this week*. First the firm is recalling sumatriptan succinate tablets in bottles and blister packs after medication samples failed to meet impurity/degradation specifications during routine testing, according to the January 22, 2020, US…
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Sun Pharmaceutical Industries Inc. is recalling dozens of lots of testosterone cypionate for injection that were manufactured under conditions similar to a previously rejected lot. The recall was published in the January 22, 2020, US Food and Drug Administration (FDA) Enforcement Report.  The…
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Customer reports of discoloration have prompted AuroMedics Pharma to pull more than 100,000 bottles of moxifloxacin ophthalmic solution, according to the January 22, 2020, US Food and Drug Administration (FDA) Enforcement Report.  The recall includes moxifloxacin ophthalmic solution 0.5%, 3-mL…
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Citing Current Good Manufacturing Practice (cGMP) violations, Wisconsin Pharmacal Company is recalling 44,373 cartons of Yeast Arrest vaginal suppositories manufactured for Vitanica and distributed in Oregon. The recall was included in the January 22, 2020, US Food and Drug Administration (FDA)…
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AvKare Inc. has initiated a voluntary recall for nearly 4000 cartons of dutasteride capsules. Among other drugs that were recalled this week*, the January 22, 2020 US Food and Drug Administration (FDA) Enforcement Report shows that samples of this medication failed to meet impurity specifications…
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