Alerts

Cyclin-dependent kinase 4/6 (CDK 4/6) inhibitors can cause lung inflammation when used to treat advanced breast cancers.

Recall of Natpara (parathyroid hormone) for Injection by Takeda due to particulate.

Recall of quinacrine dihydrochloride 25 g, 50 g, 500 g by Darmerica due to labeling error.

Recall of human sterile drug products by KRS Global Biotechnology due to lack of sterility assurance.

Recall of bacteriostatic water for Injection USP by Hospira due to potential for lack of sterility assurance.

Recall of Metrix Secure EVA dual chamber and Baxter ExactaMix by Metrix Company due to potential for leaking of the IV bag.

Recall of Milk of Magnesia oral suspension 2400 mg/30 mL by Plastikon Healthcare Pharmacy due to microbiological specification failure.

Medications used to treat hepatitis C virus (HCV) infections containing protease inhibitors can cause further liver dysfunction in patients with liver impairment.

Recall of bevacizumab 1.25 mg/0.05 mL 31G injectable and bevacizumab 2.5 mg/0.1 mL normject TB injectable by Pacifico National dba AmEx Pharmacy due to risk of infection.

Recall of sterile compounded drug products by AmEx Pharmacy due to potential health risks.

Recall of SAPIEN 3 Ultra Delivery System by Edwards Lifesciences due to burst balloons during surgery.

Recall of RELPAX (eletriptan hydrobromide) 40 mg tablets by Pfizer due to potential microbiological contamination of non-sterile products.

Recall of Volumat MC Agilia infusion pump and Vigilant Agilia drug library by Fresenius Kabi due to alarm and multiple software errors.

New warning draws attention to the increased risk of blood clots and death associated with higher doses of tofacitinib.

Recall of PRE-TAT, Superior Pain and Itch Relief, and Soothing Sore Relief Cream and Gel Products by Ridge Properties LLC DBA Pain Relief Naturally due to microbiological contamination and superpotency.

Recall of Ellipse implantable cardioverter defibrillators by Abbott (formerly St. Jude Medical Inc.) due to exposed aluminum wires that may prevent defibrillation therapy.

Recall of Airway Kit containing Sheridan endotracheal tubes by Centurion Medical Products due to potential for disconnection of the patient from the breathing circuit.

Recall of QIAsymphony SP/AS Instruments filter tips by QIAGEN due to potential to leak.

Recall of drospirenone and ethinyl estradiol tablets, USP, 3 mg/ 0.02mg by Jubilant Cadista Pharmaceuticals due to out of specification (OOS) dissolution results.

Recall of all drug products by Herbal Doctor Remedies due to marketing without FDA approval and concerns with manufacturing practices.

Recall of intra-aortic balloon pumps by Maquet/Datascope due to potential battery failure.

Recall of Kogenate FS antihemophilic factor (recombinant) by Bayer due to mislabeled drug vial.

Recall of Alaris pump model 8100 infusion sets by Becton Dickinson due to faster than expected delivery of medication.

Recall of neonatal ConchaSmart Breathing Circuit by Teleflex due to circuit cracks.