2011 Drug Recalls

December 21, 2011 McNeil Recall of Motrin IB Tablets and Caplets

December 02, 2011 Eagle Pharmaceuticals, Inc. Recalls 4 Lots of Argatroban Injection 50 mg/50 mL (1 mg/mL) Due to a Potential for Visible Particulates

October 19, 2011 Insight Pharmaceuticals Recalls "Nostrilla Nasal Decongestant" Due To Bacterial Contamination

October 03, 2011 Superior Metabolic Technologies Inc Recalls Uprizing 2.0 Because the Product Contains Superdrol, Which is a Synthetic Steroid, Making it an Unapproved New Drug

September 15, 2011 Qualitest Pharmaceuticals Issues a Nationwide Voluntary Recall of Oral Contraceptives

August 24, 2011 H and P Industries, Inc. Recalls All Lots of Povidone Iodine Swabsticks, Povidone Iodine Prep Solutions, Povidone Iodine Scrub Solutions, and Povidone Iodine Prep Gel

August 02, 2011 American Regent, Inc. Initiates Voluntary Recall of Seventeen Lots of Vasopressin Injection, USP, Multiple Dose Vials Due to Sub-Potency

July 18, 2011 American Regent Initiates Voluntary Nationwide Recall of Calcium Gluconate Injection, USP, 10%, 100 mL Pharmacy Bulk Package Due to Particulates

June 28, 2011 McNeil Consumer Healthcare Announces Voluntary Recall Of One Product Lot Of TYLENOL ® Extra Strength Caplets 225 Count Distributed In The U.S.

June 24, 2011 Qualitest Pharmaceuticals Recalls Four Lots of Butalbital, Acetaminophen, and Caffeine Tablets, USP 50mg/325mg/40mg and Four Lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5mg/500mg

June 24, 2011 Endo Pharmaceuticals Recalls Two Lots of Endocet (Oxycodone/Acetaminophen, USP) Tablets, 10 MG / 325 MG

June 22, 2011 Nature Relief is Conducting a Voluntary Recall of Nature Relief Instant Wart and Mole Remover

June 17, 2011 Ortho-McNeil-Janssen Pharmaceuticals, Inc. Voluntarily Recalls One Lot of RISPERDAL® Tablets and One Lot of Risperidone Tablets

June 15, 2011 American Regent Recalls Concentrated Sodium Chloride Injection, USP, 23.4%, 30 mL Single Dose Vial Due to Particulates

June 06, 2011 American Regent Recalls Methyldopate HCL Injection, USP 5 mL Single Dose Vial Due to Glass Particulates

June 01, 2011 Aidapak Services, LLC Recalls ALL Repackaged Pharmaceuticals by Aidapak Services, LLC Due to Potential Cross Contamination with Beta Lactam Products

May 19, 2011 American Regent Initiates Nationwide Voluntary Recall of Sterile Water for Injection, USP 50 mL Single Dose Vial Due to Particulate Matter

May 05, 2011 American Regent Recalls Caffeine and Sodium Benzoate Injection, USP 250 mg/mL, 2 mL Single Dose Vial

May 02, 2011 Bristol-Myers Squibb Recalls Coumadin (Warfarin Sodium) Crystalline 5 mg Tablets, Lot Number 9H49374A

April 26, 2011 American Regent Initiates Voluntary Nationwide Recall of Ammonium Molybdate Injection, USP (Molybdenum 250mcg/10 mL) 10 mL Single Dose Vial

April 14, 2011 Ortho-McNeil Neurologics Voluntarily Recalls Two Lots of TOPAMAX® March 29, 2011 CDC And ADPH Investigate Outbreak At Alabama Hospitals; Products Recalled

March 26, 2011 Greenstone Recalls Citalopram and Finasteride Due to Possible Mislabeling

March 25, 2011 APP Pharmaceuticals Issues A Nationwide Voluntary Recall Of Irinotecan Hydrochloride Injection

March 16, 2011 American Regent Initiates Voluntary Nationwide Recall of Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 1 mL Single Dose Vials; 5 mL and 30 mL Multiple Dose Vials

March 15, 2011 H and P Industries, Inc. Recall of All Lots of Povidine Iodine Prep Pads

March 15, 2011 American Regent Recalls Bacteriostatic Sodium Chloride Injection, USP, 0.9% 30 mL Multiple Dose Vials

March 05, 2011 OTC DRUG Nationwide Recall--Important information for patients about IV PREP Antiseptic Wipes

February 18, 2011 Upsher-Smith Laboratories Announces Expansion of Voluntary Nationwide Recall. Affected Products Include Amantadine, Amlodipine, Androxy, Baclofen, Bethanechol, Jantoven® and Oxybutynin

February 16, 2011 Upsher-Smith Laboratories Recalls Jantoven® Warfarin Sodium Tablets, USP, 3mg, Due To Mislabeled Bottles

February 05, 2011 Qualitest Pharmaceuticals Recalls Hydrocodone Bitartrate and Acetaminophen Tablets and Phenobarbital Tablets

February 04, 2011 Watson Announces Important Action Related to Nationwide Recall of Triad Alcohol Prep Products Included in Products

February 03, 2011 American Regent Recalls Potassium Phosphates Injection, USP 15 mM/5 mL Phosphorus; 22 mEq/5 mL Potassium 5 mL Single Dose Vial, Lot# 0048

January 26, 2011 Pfizer Inc. And Progenics Alert Physicians And Patients To Information Related To Triad Group Alcohol Prep Products Included In U.S. RELISTOR Kit Packaging

January 24, 2011 Important information for ARIXTRA® Starter Kit patients regarding Triad Group’s alcohol prep products

January 14, 2011 McNeil Consumer Healthcare Initiates Voluntary Recall Of Certain Over-The-Counter (OTC) Products

January 13, 2011 Genentech Informs Customers Of Important Information About Triad Groups

January 10, 2011 Important Information for Extavia® (interferon beta 1-b) Patients Regarding Triad Group's Alcohol Prep Products

January 20, 2011 Important Information for Betaseron® (interferon beta 1-b) Consumers Regarding Triad Group’s Alcohol Prep Products

January 06, 2011 Teva Pharmaceuticals, U.S.A issues a voluntary nationwide recall of Metronidazole Tablets USP, 250mg Due to Low Weight Tablets

January 05, 2011 Triad Group Issues a Voluntary Nationwide Recall of All Lots of Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks Due to Potential Microbial Contamination