Sandoz, Inc. Recalls Two Lots of Injectable Methotrexate
5/23/2013
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Those Johnson & Johnson (JNJ) Recalls Keep on Coming: Tylenol Bottles Yanked From Brazil
5/23/2013
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Takeda Pharmaceutical Co. Ltd. (TKPYY) Recalls Batch of Anemia Therapy Rienso in Switzerland After Patient Death
5/22/2013
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API's From Co's Including Cobalt Pharmaceuticals Contaminated at Chinese CMO Leads to Canadian Recalls
5/22/2013
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Health Canada: Three Companies Recall Antipsychotic Drug Quetiapine
5/20/2013
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Distributor Recalls Hospira, Inc. (HSP) Injectable Drugs on Health Risks
5/13/2013
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FDA Warns on Use of Certain Migraine Drugs During Pregnancy, Including Abbott Laboratories (ABT)' Depacon and Noven's Stavzor
5/7/2013
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Johnson & Johnson (JNJ) Licence Revoked Over Baby Powder Concerns
5/6/2013
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Johnson & Johnson (JNJ) Halts Tylenol Production in South Korea Over Mishap
5/6/2013
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Boehringer Ingelheim Corporation's Anticoagulant Pradaxa Adds Warning to Prescribing Info
4/30/2013
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Hospira, Inc. (HSP) Recalls Piperacillin and Tazobactam for Injection Due to Precipitation/Crystallization
4/30/2013
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Takeda Pharmaceutical Co. Ltd. (TKPYY) Penalized Over Quality Failure
4/22/2013
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FDA Still Allow People to Take PRACS Institute (Formerly known as Cetero Research)'s Unapproved Drug
4/16/2013
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Waiter, There's Cardboard in My Sample: FDA Warns Pfizer Inc. (PFE) Over Manufacturing Gaffes
4/12/2013
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GlaxoSmithKline (GSK)'s Avandia Gets Second Look at Heart Risk by U.S.
4/12/2013
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Pfizer Inc. (PFE) Recalls Thyroid-Disorder Drug Over Odor Problem
4/5/2013
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Alexion Pharmaceuticals Inc. (ALXN) Gets FDA Warning Over Contamination at RI Plant
4/2/2013
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Brass Particulates, Sealing Issues Cause Two More Hospira, Inc. (HSP) Injection Recalls
4/2/2013
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Apotex Inc. is in the FDA Dog House, Again
3/21/2013
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Clinical Specialties Recalls Eye Drugs in Another Sterility Scare
3/21/2013
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Dr. Reddy's Laboratories, Inc. (RDY) and Glenmark Pharmaceuticals Recall Drugs in U.S. Over Odors
3/19/2013
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FDA Investigates Safety of Merck & Co., Inc. (MRK)'s Januvia and Bristol-Myers Squibb Company (BMY)'s Byetta
3/18/2013
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IMPAX Laboratories, Inc. (IPXL) Continues to Ignore FDA Warnings, Causing Delays
3/18/2013
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Heart Warning Added to Pfizer Inc. (PFE)s "Z-Pak" Antibiotic by FDA
3/13/2013
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Salmon Hormone Sold by Novartis AG (NVS), Upsher-Smith Laboratories and More May Contain Too Much Cancer Risk
3/5/2013
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Affymax, Inc. (AFFY) Plunges After Recall of Omontys Due to Deaths
2/27/2013
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Ranbaxy Laboratories (RANBAXY.BO) Slams Consumers for Seeking Lipitor Recall
2/25/2013
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Mobius Theraputics™ Provides Update on Recall of Two Lots of Mitosol®
2/20/2013
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Gilead Sciences, Inc. (GILD) Issues a Voluntary Recall of One Lot of Vistide®
2/19/2013
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FDA Seizes Tainted Dietary Supplements From Globe All Wellness LLC
2/15/2013
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FDA Issues Another Warning on Fake Version of Roche (RHHBY)'s Avastin
2/8/2013
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Novo Nordisk A/S (NVO): Previously Announced FDA Warning Letter Published
2/5/2013
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Novartis AG (NVS) Recalls More OTC Meds
2/1/2013
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France Suspends Sales of Bayer AG (BAY.F)'s Acne Pill Diane 35 After Deaths
1/31/2013
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Hospira, Inc. (HSP) Recalls One Lot of Electrolyte Solution After Mold Found
1/29/2013
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FDA Warns of Liver Injury Risk With Otsuka America Pharmaceutical, Inc.'s Tolvaptan
1/25/2013
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Advance Pharmaceutical Issues Nationwide Voluntary Recall of One Lot of Ferrous Sulfate Tablets
1/18/2013
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Is AbbVie (ABBV) Already Making a Recall?
1/16/2013
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Mobius Theraputics™ Issues a Voluntary Recall of Mitosol®
1/10/2013
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Johnson & Johnson (JNJ) Diabetes Pill May Have Heart Risks, FDA Staff Says
1/10/2013
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Fake Allergan Inc. (AGN) Botox Warning by FDA to 350 Medical Practices
12/27/2012
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Mylan Inc. (MYL) Recalls Painkiller Pills Due to Risk of Higher Dosage
12/27/2012
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Vertex Pharmaceuticals Incorporated (VRTX) Discloses Hep C Drug Deaths
12/26/2012
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FDA Warns Against Boehringer Ingelheim Pharmaceuticals, Inc.'s Pradaxa in Patients With Mechanical Prosthetic Heart Valves
12/20/2012
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Performance Plus Marketing Recalling Supplements for Unapproved New Drugs
12/19/2012
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Matrixx Initiatives, Inc. (MTXX) Issues Nationwide Voluntary Recall of One Lot of Zicam®
12/19/2012
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Hospira, Inc. (HSP) Issues Voluntary Nationwide Recall of Three Lots of Carboplatin Injection Due to Visible Particulate Matter
12/17/2012
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Bayer HealthCare (BAY) Consumer Care Voluntarily Recalls 56 Lots of BRONKAID Caplets
12/10/2012
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FDA Withdraws Generic Budeprion
12/7/2012
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GlaxoSmithKline (GSK)'s High-Dose Zofran Pulled From Market
12/7/2012
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Qualitest Pharmaceuticals Issues Voluntary, Nationwide Recall of Hydrocodone Bitartrate and Acetaminophen Tablets
12/7/2012
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LifeVantage Corporation (LFVN) Announces Voluntary Recall and Replacement of Select Lots of Protandim ® Dietary Supplement
12/6/2012
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FDA Rejects Request to Ban Lice Shampoo for Kids
11/30/2012
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Aurobindo Pharma Drug Recalled in the U.S.
11/29/2012
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Ranbaxy Laboratories (RANBAXY.BO) Recall Brings Back Painful Memories
11/27/2012
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FDA: 5-Hour Energy Drink Linked to Deaths
11/16/2012
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Boehringer Ingelheim Corporation Initiates a Voluntary Recall of a Single Manufacturing Lot of Pradaxa®
11/7/2012
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GlaxoSmithKline (GSK) Pulls Vaccine Batch in Canada Over Contamination Concerns
11/7/2012
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FDA: No Increased Bleeding Risk for Boehringer Ingelheim GmbH's Pradaxa
11/2/2012
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Precautionary Holds on Novartis AG (NVS)' Influenza Vaccines Lifted in Canada, Switzerland
11/1/2012
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Ameridose Issues Recall of All Products
11/1/2012
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France Halts Sale of Novartis AG (NVS) Flu Vaccine, Germany Orders Recall
10/26/2012
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Italy Bans Four Novartis AG (NVS) Flu Vaccines Amid Side-Effects Probe
10/25/2012
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European Medicines Agency Probes Roche (RHHBY) for Reporting Failures
10/25/2012
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FDA: Improper Use of Endo Pharmaceuticals (ENDP) Drug Could Cause Death
10/15/2012
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FDA Recalls Hospira, Inc. (HSP)'s Lactated Ringer's and 5% Dextrose Injection, 1000 Ml, Flexible Containers
10/9/2012
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UK Says Sanofi (France) (SAN.PA), Merck & Co., Inc. (MRK) Recall Some Typhoid Vaccine Batches
10/9/2012
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FDA: Teva Pharmaceutical Industries Limited (TEVA) Antidepressant is Ineffective
10/9/2012
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FDA: New England Compound Center Drugs Tied to Meningitis
10/8/2012
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Watson Laboratories, Inc. (WPI) Recalls Two Lots of Hydrocodone Pain Drug
9/24/2012
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Bioniche Life Sciences Inc. (BNC) Discovers a Counterfeit Equine Product
9/24/2012
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Baby Deaths Linked to SimplyThick's Infant Formula Additive, FDA Cautions
9/20/2012
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FDA: Boehringer Ingelheim Pharmaceuticals, Inc.s' Parkinson's Drug May Have Possible Risk of Heart
9/20/2012
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Bedford Laboratories Broadens Voluntary Recall of Leucovorin Calcium Injection USP
9/18/2012
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FDA Warns of Burns From OTC Pain and Muscle Relievers Including Johnson & Johnson (JNJ)'s Bengay and Sanofi (France) (SAN.PA)'s Icy Hot
9/17/2012
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Qualitest Pharmaceuticals Issues Voluntary, Nationwide Recall for One Lot of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg Due to the Potential for Oversized Tablets
9/11/2012
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Sun Pharmaceutical Industries Ltd Issues Nationwide Voluntary Recall of One Lot of Nimodipine Capsules Due to Crystallization of the Fill Material
9/4/2012
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Bristol-Myers Squibb Company (BMY) Recalls Vials of Cancer Drug
9/4/2012
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FDA Warns Against Using Pfizer Inc. (PFE)'s Revatio in Children
8/31/2012
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FDA Warns of Possible Cataract Link With Vertex Pharmaceuticals (MA) (VRTX)'s Kalydeco
8/30/2012
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Sanofi (France) (SAN.PA) Recalls Nine Lots of Kidney Transplant Rejection Drug
8/28/2012
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European Medicines Agency Agency Recalls Pacira Pharmaceuticals, Inc. Drug on Contamination Worries
8/27/2012
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Hospira, Inc. (HSP) Recalls Pain Injectable on Overdose Risk
8/17/2012
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FDA: Codeine Can be Fatal to Some Children
8/16/2012
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Fresenius Medical Care's Leaked Internal Memo Leads to FDA Class I Recall
8/2/2012
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FDA Warns About Seizures With Acorda Therapeutics (ACOR)' MS Drug Ampyra
7/24/2012
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Johnson & Johnson (JNJ) Recalls Some Duragesic Pain Patches
7/20/2012
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Hospira, Inc. (HSP) Recalls Cancer Drugs for Glass Particles
7/17/2012
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Health Canada: GlaxoSmithKline (GSK) Issues Warning on Pulmonary Arterial Hypertension Drug
7/16/2012
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Pfizer Inc. (PFE) Recalls Robitussin Product Due to Label Errors
7/12/2012
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MAQUET Initiates Class I Recall of the FLOW-i Anesthesia System
7/6/2012
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Bedford Laboratories Issues Nationwide Voluntary Hospital/User-Level Recall of Leucovorin Calcium Injection
7/5/2012
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Johnson & Johnson (JNJ) Recalls KY Liquibeads
7/5/2012
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Roche (RHHBY) Ignores 80,000 Cases of Possible Adverse Drug Reactions
7/3/2012
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Bedford Laboratories Issues Voluntary Drug Recall
6/29/2012
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Heart Risk Seen With GlaxoSmithKline (GSK)'s Zofran?
6/29/2012
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Health Canada Warns Hospira, Inc. (HSP) Over Paclitaxel Batches
6/28/2012
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Merck & Co., Inc. (MRK) Recalls Vaccine After Accidental Release: FDA
6/25/2012
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CSL Limited (CMXHF.PK): Viral Component Likely Cause of Convulsions in Kids Given Fluvax
6/21/2012
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Sanofi Pasteur (SASY.PA) Recalls Tuberculosis Vaccine Over Contamination Concerns
6/18/2012
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Novartis AG (NVS) Recalls Introvale Birth Control Pills Over Packaging Flaw
6/8/2012
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FDA Asked to Ban Lice Shampoo for Kids
6/4/2012
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FDA Warns Johnson & Johnson (JNJ) Over Vaginal Products
5/31/2012
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FDA Warns Consumers About Fake Versions of Teva Pharmaceutical Industries Limited (TEVA)'s Adderall
5/30/2012
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Breathe Deeply: Safety Concerns Over Boehringer Ingelheim Corporation's Spiriva
5/25/2012
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Frank's Pharmacy Recalls Sterile Human, Veterinary Prescriptions
5/25/2012
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Allergy Therapeutics plc: Notification of Voluntary Product Recall of Anapen® by Lincoln Medical
5/23/2012
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Pfizer Inc. (PFE) Recalls 650,000 Bottles of Advil Liqui-Gels
5/21/2012
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Johnson & Johnson (JNJ) Recalls Nearly 54,000 Packages of Imodium
5/21/2012
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Hospira, Inc. (HSP) Recalls Pain Drug Cartridges
5/16/2012
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FDA Says Unsure if Novartis AG (NVS) MS Pill Caused Deaths
5/15/2012
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FDA Voices Caution About Popular Bone Drugs, Including Novartis AG (NVS)'s Reclast
5/11/2012
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Lethal Injection Drug from Naari AG Held by Nebraska is Recalled
5/10/2012
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FDA Warns Not to Mix Merck & Co., Inc. (MRK) Hep C Drug With HIV Meds
4/27/2012
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American Regent, Inc. Initiates Nationwide Voluntary Recall of Epinephrine Injection, USP, 1:1000, 1 mL Ampules Lot #1395 Due to Discoloration and Small Visible Particles
4/25/2012
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FDA Issues Warning Over Fentanyl Patches; Makers Include Mylan Inc. (MYL) and Watson Pharmaceuticals, Inc. (WPI)
4/23/2012
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Novo Nordisk A/S (NVO) Warns FDA of Biosimilar Concerns
4/19/2012
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American Regent, Inc. Initiates Nationwide Voluntary Recall of Cyanocobalamin Injection, USP, 1000 mcg/mL, 1mL Vial Lot #s 1662, 1679, 1683 Due to Cracks in the Vials
4/3/2012
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Sun Pharmaceutical Industries Ltd Recalls 1,55,000 Eye Solution Bottles From US
3/30/2012
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FDA Adds Warnings to Forest Laboratories, Inc. (FRX)' Celexa Label
3/28/2012
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IntelliCell BioSciences (SVFC) Receives Raft of FDA Warnings
3/28/2012
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Diabetics in Danger After Drug Sparks Health Alert, Irish Medicines Board Reveals
3/16/2012
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FDA Issues Warning Letter to Warner Chilcott, PLC (WCRX) Suggesting Subpotent Birth Control Pills Problem
3/14/2012
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Troubled Boehringer Ingelheim Corporation Unit, Bedford Laboratories Recalls Leukemia Medicine
3/12/2012
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FDA Adds a Warning, Removes Another From Statin Labels Including Pfizer Inc. (PFE)'s Lipitor
3/1/2012
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Merck & Co., Inc. (MRK) Warned by FDA on Failure to Study Januvia for Side Effects
3/1/2012
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Pfizer Inc. (PFE) Recalls Expired Lot of Prevnar Vaccine
2/29/2012
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GlaxoSmithKline (GSK) Recalls Drug Made at Troubled Novartis AG (NVS) Plant
2/28/2012
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Regeneca International, Inc. Issues a Voluntary Nationwide Recall of All Lots of Single Capsule RegenErect Because of Potential Health Risks
2/27/2012
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FDA Issues Import Alerts for 22 Chinese Heparin Suppliers
2/24/2012
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American Regent, Inc. Initiates Nationwide Voluntary Recall of Phenylephrine HCl Injection, USP, 1%, 5 mL Vial, Lot# 0693, Due to Visible Particles
2/23/2012
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Novartis AG (NVS) to Add Warnings to Rasilez Blood-Pressure Drug
2/20/2012
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Sanofi (France) (SAN.PA)'s Genzyme Corporation (GENZ) Recalls 9,380 Vials of Fludara Leukemia Drug Made at Ben Venue Laboratories Plant
2/20/2012
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McNeil Consumer Healthcare Announces Voluntary Nationwide Recall of Infants' TYLENOL® Oral Suspension, 1 oz. Grape Due to Dosing System Complaints
2/20/2012
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Bedford Laboratories Issues Nationwide Voluntary Recall of Cytarabine for Injection, USP, 1 Gram Per Vial
2/16/2012
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Roche (RHHBY) Warns of Counterfeit Avastin in the U.S.
2/16/2012
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Regeneca International, Inc. Recalls Specific Lot of RegenArouse Because of Potential Health Risks
2/13/2012
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FDA Warning: Stomach Acid Drugs Including AstraZeneca PLC (AZN)'s Nexium and Santarus Inc. (SNTS)'s Zegerid, Increase Risk of Bacterial Infections
2/10/2012
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Cadence Pharmaceuticals, Inc. Announces Voluntary Recall of One Lot of OFIRMEV® (Acetaminophen) Injection
2/7/2012
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Bedford Laboratories Issues a Voluntary Nationwide Patient Level Recall of Acetylcysteine Solution, USP, Lot 1877093
2/2/2012
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Pfizer Inc. (PFE) Recalls 1 Million Birth Control Packs After Mixup
2/2/2012
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Teva Pharmaceutical Industries Limited (TEVA)'s Cephalon, Inc. (CEPH) Recalls Treanda Leukemia Drug Due to Glass Fragments
1/31/2012
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Seattle Genetics, Inc. (SGEN) Lymphoma Drug Gets Boxed Warning on Brain Infection Risk
1/18/2012
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Bedford Laboratories Issues Guidance on 2011 Voluntary Recall of Polymyxin B for Injection USP and Vecuronium Bromide for Injection Related to Glass Particulates
1/11/2012
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Novartis AG (NVS) Unit to Take $120 Million Charge on Recall, Initiates Precautionary Recall of 4 OTC Brands
1/10/2012
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Johnson & Johnson (JNJ) Recalls 12 Million Bottles of Motrin That May Not Dissolve
12/22/2011
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FDA Further Restricts Use of Sanofi (France) (SAN.PA)'s Multaq
12/21/2011
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Neti Pots Linked to Brain-Eating Amoeba Deaths
12/20/2011
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Novartis AG (NVS): Patient Died After Starting Gilenya
12/15/2011
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FDA: U.S. Marshals Seize Products Containing Banned Ephedrine for Dietary Supplements
12/7/2011
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Bayer AG (BAY.F) Concealed Yasmin's Clot Risk, Former FDA Chief Says
12/7/2011
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FDA, Federal Trade Commission Act to Remove "Homeopathic" HCG Weight Loss Products from the Market
12/6/2011
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FDA: U.S. Marshals Seize Dietary Supplements, Drugs Manufactured by Syntec Inc.
12/2/2011
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Naari AG Wants Nebraska to Return Lethal Injection Drug
11/30/2011
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EU Recalls Cancer Meds Made by Boehringer Ingelheim Corporation Unit
11/28/2011
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Boehringer Ingelheim Corporation Says About 260 Deaths Related to Pradaxa
11/16/2011
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Boehringer Ingelheim Corporation Says About 50 Deaths Related to Pradaxa
11/4/2011
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Group: Johnson & Johnson (JNJ)'s Baby Shampoo a Cancer Risk
11/3/2011
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FDA Cites Blood-Clot Risk Tied to Bayer AG (BAY.F) Birth-Control Pills
10/31/2011
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Side Effects Prompt European Recall of Baxter Healthcare Corporation (BAX)'s Flu Vaccine Preflucel
10/31/2011
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Eli Lilly and Company (LLY) to Withdraw Xigris From Market Worldwide
10/26/2011
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Insight Pharmaceuticals Issues a Voluntary Nationwide Recall of "Nostrilla Nasal Decongestant" Due to Bacterial Contamination
10/20/2011
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Ranbaxy Laboratories (RANBAXY.BO) Recalls Three Drugs From UK Market
10/17/2011
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Bristol-Myers Squibb Company (BMY)'s Sprycel May Increase Hypertension Risk, FDA Says
10/12/2011
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Celgene (CELG) Asked to Specify Revlimid Cancer Risk
10/6/2011
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New Label on Genentech (RHHBY)'s Avastin Warns of Infertility
10/5/2011
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CSL Limited (CMXHF.PK) Denies Report of New Manufacturing Warnings from FDA
9/29/2011
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Will the FDA Yank Bayer HealthCare Pharmaceuticals (BAYA.F)'s Risky Birth-Control Pill Yaz?; FDA Continues to Monitor Clot Risk Six Months Later
9/28/2011
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GlaxoSmithKline (GSK)'s Alli Under Review Over Liver Failure Fears
9/26/2011
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VA Halts Roche (RHHBY)'s Avastin for Eye Disease; Rival Regeneron Pharmaceuticals, Inc. (REGN)'s Stock Surges
9/23/2011
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EU Agency Calls for Restrictions on Sanofi (France) (SASY.PA)'s Multaq
9/23/2011
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Vaccine Maker CSL Limited (CMXHF.PK) Downplays Link to Side Effects
9/21/2011
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GlaxoSmithKline (GSK) Anti-Nausea Drug Linked to Arrhthymias
9/19/2011
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Qualitest Pharmaceuticals Pharma Recalls Oral Contraceptives
9/16/2011
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Daiichi Sankyo, Inc. (D4S.F) Unit Warned by FDA Over Manufacturing
9/14/2011
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GlaxoSmithKline (GSK) Stops Tykerb Arm of Breast-Cancer Trial
9/13/2011
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Boehringer Ingelheim Corporation's Pradaxa Causes a Side Effect Flap in New Zealand
9/12/2011
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FDA Updates Boxed Warning for TNF-alpha Inhibitors
9/8/2011
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FDA Warns of Severe Allergy Risk with Merck & Co., Inc. (MRK) Antipsychotic
9/6/2011
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SANE Vax, Inc. Reports Human Papillomavirus (HPV) DNA Contamination in Gardasil(TM) to FDA: Requests Public Safety Investigation
9/6/2011
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FDA: Novartis Corporation (NVS)'s Osteoporosis Drug Reclast Raises Kidney Failure Risk
9/6/2011
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Pfizer Inc. (PFE) Anti-Smoking Drug Tied to Blackouts
9/2/2011
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Roche (RHHBY) Avastin Injections Linked to Blindness
9/1/2011
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Bristol-Myers Squibb Company (BMY)'s Sprycel Linked to Potentially Fatal Side-Effect: Health Canada Reports
9/1/2011
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U.K. Warns of Package Mix-Up Between AstraZeneca PLC (AZN)'s Seroquel XL and Reckitt Benckiser Plc (RB.L)'s Nurofen Plus
8/26/2011
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FDA: High Doses of Forest Laboratories, Inc. (FRX)'s Celexa Linked to Abnormal Heart Rhythms
8/26/2011
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H&P Industries, Inc. Issues a Voluntary Recall of All Lots of Povidone Iodine Swabsticks, Povidone Iodine Prep Solutions, Povidone Iodine Scrub Solutions, and Povidone Iodine Prep Gel
8/25/2011
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Advocacy Group to FDA: Acid Reflux Drugs Should Have Black Box Warnings
8/25/2011
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Johnson & Johnson (JNJ) Recalls Nearly 2.5 Million Packages of Tylenol Cold Gelcaps
8/17/2011
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Deaths Prompt Revisions in Japanese Precautions for Boehringer Ingelheim Corporation's Prazaxa
8/16/2011
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Dr. Reddy's Laboratories, Inc. (RDY) Recalls Contaminated Simvastatin in the US
8/15/2011
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FDA OKs Stronger Warning for Takeda Pharmaceutical Co. Ltd. (TKDG.DE)'s Diabetes Drug Pioglitazone
8/9/2011
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American Regent, Inc. Initiates Voluntary Recall of Seventeen Lots of Vasopressin Injection, USP, Multiple Dose Vials Due to Sub-Potency
8/5/2011
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FDA: High Doses Of Pfizer Inc. (PFE)'s Antifungal Drug Fluconazole Might Cause Birth Defects
8/4/2011
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FDA Warns of Fluter Domull's Counterfeit "Morning-After" Pill
8/2/2011
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FDA Report Finds Shrink Wrap in Merck & Co., Inc. (MRK) Vaccines
8/1/2011
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Pfizer Inc. (PFE)'s Zyvox and Antidepressants May Be Fatal Combination
7/27/2011
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FDA Issues Alerts on Sanofi (France) (SASY.PA)'s Heart Drug Multaq
7/22/2011
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European Medicines Evaluation Agency Warns About Takeda Pharmaceutical Co. Ltd. (TKDG.DE)'s Actos, Backs Pfizer Inc. (PFE)'s Champix, Restricts GlaxoSmithKline (GSK)'s Pandemrix
7/22/2011
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AstraZeneca PLC (AZN) Puts Heart Warning on Anti-Psychotic Seroquel
7/20/2011
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