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FDA recalls blood pressure medicine due to potential cancer risk
FDA recalls blood pressure medicine due to potential cancer risk

Teva Recalls U.S.-Made Drugs Following Contamination Fears | 2021-10-04 | SupplyChainBrain
Teva Recalls U.S.-Made Drugs Following Contamination Fears | 2021-10-04 | SupplyChainBrain

FDA recall expands for heart drug with possible cancer-causing impurity
FDA recall expands for heart drug with possible cancer-causing impurity

Teva's troubled Godollo plant earns firm US FDA warning letter
Teva's troubled Godollo plant earns firm US FDA warning letter

FDA Recall Watch | McIntyre Law PC
FDA Recall Watch | McIntyre Law PC

Teva Recalls One Lot Of IDArubicin Hydrochloride Injection
Teva Recalls One Lot Of IDArubicin Hydrochloride Injection

Teva recalls US-made drugs following contamination fears - The Boston Globe
Teva recalls US-made drugs following contamination fears - The Boston Globe

Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules | DAIC
Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules | DAIC

Valsartan Blood Pressure Meds Recalled | PrimeMED
Valsartan Blood Pressure Meds Recalled | PrimeMED

Teva Pharma Receive Warning Letter - Parker Waichman LLP
Teva Pharma Receive Warning Letter - Parker Waichman LLP

2 high blood pressure medications added to recall of heart drug - ABC News
2 high blood pressure medications added to recall of heart drug - ABC News

Teva Pharmaceuticals announces recall of two blood pressure drugs.
Teva Pharmaceuticals announces recall of two blood pressure drugs.

FDA announces recall of platelet-reducing medication due to risk of clotting or other adverse cardiovascular outcomes
FDA announces recall of platelet-reducing medication due to risk of clotting or other adverse cardiovascular outcomes

RECALL ALERT: FDA Adds to List of Recalled Blood Pressure Drugs - The Diabetes Site News
RECALL ALERT: FDA Adds to List of Recalled Blood Pressure Drugs - The Diabetes Site News

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
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

Vegas doctor explains blood pressure med recall
Vegas doctor explains blood pressure med recall

Teva recall: Tainted blood pressure drugs continue to show up in U.S. supply | Fierce Pharma
Teva recall: Tainted blood pressure drugs continue to show up in U.S. supply | Fierce Pharma

Overview of the FDA's Drug-Recall Process
Overview of the FDA's Drug-Recall Process

Teva Recalls Drug Vials, Shuts Facility Over Mold Concerns - TheStreet
Teva Recalls Drug Vials, Shuts Facility Over Mold Concerns - TheStreet

Dissolution Test Failure Prompts Recall of Anagrelide Capsules - MPR
Dissolution Test Failure Prompts Recall of Anagrelide Capsules - MPR

Teva Stops Production At US Plant After FDA Concerns: Report
Teva Stops Production At US Plant After FDA Concerns: Report

Teva recalls 2 lots of hypertension drug on dissolution issues
Teva recalls 2 lots of hypertension drug on dissolution issues

Metformin recall by FDA: What's the latest news on metformin ER?
Metformin recall by FDA: What's the latest news on metformin ER?

Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure | FDA
Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure | FDA

Teva halts output at U.S. drug plant after FDA flags concerns | Reuters
Teva halts output at U.S. drug plant after FDA flags concerns | Reuters

Teva recalls one lot of leukemia med after finding particulates in vial | Fierce Pharma
Teva recalls one lot of leukemia med after finding particulates in vial | Fierce Pharma

Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure
Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure