Recalls involving N-Nitrosodimethylamine (NDMA) content.
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Recent Recalls involving devices.
Recalls involving hand sanitizer.
Recalls involving undeclared sildenafil and/or tadalafil.
Recall of twelve lots of CHANTIX (Varenicline) tablets by Pfizer due to N-nitroso varenicline content.
Recall of specific NEUTROGENA and AVEENO aerosol sunscreen products by Johnson and Johnson due to presence of benzene.
Recall of all sterile compounded drug products by Innoveix Pharmaceuticals due to lack of sterility assurance.
Recall of one lot of topotecan injection 4 mg/4 mL (1 mg/mL) by Teva due to presence of particulate matter.
Recall of Surgical Procedure Packs by DeRoyal Industries due to mislabeled lidocaine.
Recall of Imperia Elita Vitaccino Coffee by Dash Xclusive due to undeclared sibutramine and fluoxetine.
Recall of Levemir, Tresiba, Fiasp, Novolog and Xultophy Product Samples by Novo Nordisk due to improper storage.
Recall of Sterile Water for Injection USP by Hospira due to visible particulate.
Recall of One Lot of Bupivacaine Hydrochloride Injection USP, 0.5% and One Lot of Lidocaine HCl Injection USP, 1% by Hospira due to mislabeling.
Recall of Certain Lots of NP Thyroid (Thyroid Tablets - USP) by Acella Pharmaceuticals due to sub potency.
Recall of ChloraPrep Hi-Lite Orange 26 mL Applicator by BD due to defective applicator.
