Pravastatin Sodium Tablets Packaged in Bottles Recalled - Pharmaceutical Processing World
Drug Recall: Valsartan - MedWaste Management
FDA RECALL: Montelukast tablets - Premier Allergy
Teva's troubled Godollo plant earns firm US FDA warning letter
Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure
FDA posts a flurry of voluntary drug recalls by Teva, Glenmark, Apotex and VistaPharm
2 high blood pressure medications added to recall of heart drug - ABC News
Teva Recalls One Lot Of IDArubicin Hydrochloride Injection
Teva Stops Production At US Plant After FDA Concerns: Report
Teva recalls US-made drugs following contamination fears - The Boston Globe
FDA announces recall of platelet-reducing medication due to risk of clotting or other adverse cardiovascular outcomes
FDA Drug Recall Statistics
Teva Pharmaceuticals USA, Inc. Initiates Voluntary Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets USP 500 mg and 750 mg Due to Detection of N-Nitrosodimethylamine (NDMA) | FDA
FDA posts a flurry of voluntary drug recalls by Teva, Glenmark, Apotex and VistaPharm
Vegas doctor explains blood pressure med recall
Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure | FDA
More Blood Pressure Drugs Recalled Due to Potential Cancer Risk | Moffitt
Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules | DAIC
Blood pressure drugs: Two more medications recalled for cancer risk
IMPORTANT Metformin Hydrochloride Extended Release Tablets, USP, 500 mg and 750 mg RECALL NOTICE Dear Member, Your health is imp
FDA Safety Alert: Teva Initiates Voluntary Nationwide Recall of Specific Lots of Fentanyl Buccal Tablets CII Due to a Labeling Error - Drugs.com
Teva recalls one lot of leukemia med after finding particulates in vial | Fierce Pharma
What to Know About the 2023 Eyedrop Recalls, Understanding the Risks
Teva halts output at U.S. drug plant after FDA flags concerns
Teva Initiates Voluntary Nationwide Recall of One Lot of Topotecan Injection 4 mg/4 mL (1 mg/mL) Due to Presence of Particulate Matter | FDA
International Laboratories, LLC Issues Voluntary Nationwide Recall of One (1) Lot of Pravastatin Sodium Tablets USP, 40mg Packaged in Bottles of 30 Tablets Due to Mislabeling NDC # 54458-925-16; Lot # 115698A | FDA
