FDA•
Niacin Extended-release Tablets
Lannett is recalling 1,000 mg Niacin Extended-release Tablets due to failed dissolution specifications.
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FDA•Xyvona (levorphanol tartrate) 2mg TabletsForte BioPharma is recalling Xyvona (levorphanol tartrate) 2mg tablets due to the FDA's denial of the product's proprietary name.
2 products
FDA•LOWPred Mild Ophthalmic SuspensionAbbVie is recalling 10 mL bottles of Pred Mild ophthalmic suspension due to failed stability specifications.
FDA•LOWLidocaine HCl Injection 2%Eugia US LLC is recalling Lidocaine HCl Injection 2% single-dose vials because the label wrap obscures the barcode, preventing it from scanning.
FDA•ToxiBan Charcoal-Kaolin SuspensionLloyd Inc. is recalling ToxiBan Charcoal-Kaolin Suspension due to microbial levels exceeding specification limits.
FDA•LOWNicotine Transdermal System Patch 14 mgAveva is recalling 14 mg Nicotine Transdermal System Patches due to elevated levels of oxidative-related impurities.
FDA•LOWBusulfan InjectionSagent Pharmaceuticals is recalling Busulfan Injection (NDC 25021-241-10) due to failed impurities and degradation specifications.
FDA•LOWPrimidone Tablets 250 mgAmerican Health Packaging is recalling Primidone Tablets 250 mg distributed nationwide due to potential cross-contamination with Acemetacin.
2 products
FDA•CRITICALLactated Ringer's Injection USPB. Braun Medical is recalling Lactated Ringer's Injection USP due to the presence of particulate matter.
FDA•LOWPrimidone 50 mg TabletsGolden State Medical Supply is recalling Primidone 50 mg Tablets (NDC 51407-637-05) due to potential cross-contamination with Acemetacin.
2 products- FDA•LOWPrimidone 250mg Tablets
Lannett Company is recalling Primidone 250mg Tablets (NDC 0527-1231-01) due to potential cross-contamination with Acemetacin API.
FDA•CRITICALMG217 Multi-Symptom Treatment CreamWisconsin Pharmacal is recalling MG217 Multi-Symptom Treatment Cream due to Staphylococcus aureus contamination.
FDA•CRITICALHeritage Animal Nutrition Medicated FeedHeritage Animal Nutrition is recalling 50 lb bags of medicated feed due to potential rumensin contamination.
FDA•LOWLevocarnitine Injection, USP 1 g/5 mLAmerican Regent is recalling Levocarnitine Injection 1 g/5 mL vials (NDC 0517-1045-01) due to missing label.
FDA•LOWMonsel's Ferric Subsulfate Solution 8 mLPremier Dental Products is recalling Monsel's Ferric Subsulfate Solution 8 mL vials (NDC 48783-112-08) due to incorrect expiration date on the vial label.
FDA•LOWBuspirone Hydrochloride Tablets 5 mgUnichem is recalling 500-count bottles of Buspirone Hydrochloride Tablets, 5 mg, due to subpotency.
FDA•LOWCVS Lidocaine Wound GelCVS is recalling Lidocaine Wound Gel (NDC 59898-950, 0.5 oz) due to failed pH specifications.
FDA•LOWAmprol 25% Medicated ArticleHuvepharma is recalling one bag of Amprol 25% medicated article due to missing lot number and expiration date information.
FDA•LOWMagnesium Chloride 6-Hydrate Crystal 500GAvantor is recalling Magnesium Chloride 6-Hydrate Crystal 500G bottles (NDC 10106-2448-1) due to subpotency.
FDA•CRITICALMagnesium Sulfate in Water for Injection IV BagAmneal is recalling Magnesium Sulfate IV bags (NDC 70121-1720-3) due to product mix-up with Tranexamic Acid.
FDA•LOWRemedy Gel Hydrocortisone 1%Island Kinetics is recalling Remedy Gel hydrocortisone 1% due to subpotency.
3 products
FDA•CRITICALWebcol Alcohol Prep Pads (70% Isopropyl Alcohol)Cardinal Health is recalling Webcol Alcohol Prep Pads (200-count boxes) due to microbial contamination that may pose infection risk.
3 products
FDA•LOWGelatin Capsule Pack for Sodium Iodide I-131 KitInternational Isotopes recalling Gelatin Capsule Packs (NDC 69208-003-15/25/35) for Sodium Iodide I-131 Kit due to failed specifications.
FDA•LOWNilotinib Capsules 150 mgCipla is recalling Nilotinib Capsules 150 mg due to failed stability test results.
2 products
FDA•LOWEptifibatide Injection 75 mg/100 mLSlate Run Pharmaceuticals recalls Eptifibatide Injection 75 mg/100 mL vials (NDC 70436-027-80, 70436-163-80) due to incorrect dosing-route labeling.
FDA•CRITICALWhite Vein Advanced Alkaloids Chewable TabletsShaman Botanicals is recalling White Vein Advanced Alkaloids Chewable Tablets due to higher-than-labeled levels of 7-hydroxymitragynine.
2 products
FDA•LOWPitavastatin Tablets, 2 mgNorthstar Rx LLC is recalling Pitavastatin Tablets, 2 mg (NDC 72603-479-01) due to a foreign 1 mg tablet found in bottles.
FDA•LOWDoxazosin Tablets, USP 4 mgUnichem is recalling Doxazosin Tablets 4 mg (NDC 29300-353-10) due to incorrect tablet imprinting that may cause medication errors.
FDA•CRITICALUDENYCA Pegfilgrastim-cbqv InjectionUDENYCA pegfilgrastim-cbqv prefilled syringes (Lot 2199821) recalled due to improper storage temperature.