Drug Recalls

Miami Drug Recalls Attorneys

If you’d like more information on these and other drug recalls, please visit the FDA Website.

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Aidapak Services, LLC Recalls ALL Repackaged Pharmaceuticals by Aidapak Services, LLC Due to Potential Cross Contamination with Beta Lactam Products (June 01, 2011)
American Regent, Inc. Initiates Voluntary Recall of Seventeen Lots of Vasopressin Injection, USP, Multiple Dose Vials Due to Sub-Potency (August 02, 2011)
American Regent Initiates Voluntary Nationwide Recall of Calcium Gluconate Injection, USP, 10%, 100 mL Pharmacy Bulk Package Due to Particulates (July 18, 2011)
American Regent Recalls Concentrated Sodium Chloride Injection, USP, 23.4%, 30 mL Single Dose Vial Due to Particulates (June 15, 2011)
American Regent Recalls Methyldopate HCL Injection, USP 5 mL Single Dose Vial Due to Glass Particulates (June 06, 2011)
American Regent Initiates Nationwide Voluntary Recall of Sterile Water for Injection, USP 50 mL Single Dose Vial Due to Particulate Matter (May 19, 2011)
American Regent Recalls Caffeine and Sodium Benzoate Injection, USP 250 mg/mL, 2 mL Single Dose Vial (May 05, 2011)
American Regent Initiates Voluntary Nationwide Recall of Ammonium Molybdate Injection, USP (Molybdenum 250mcg/10 mL) 10 mL Single Dose Vial (April 26, 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 16, 2011)
American Regent Recalls Bacteriostatic Sodium Chloride Injection, USP, 0.9% 30 mL Multiple Dose Vials (March 15, 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 (February 03, 2011)
APP Pharmaceuticals Issues A Nationwide Voluntary Recall Of Irinotecan Hydrochloride Injection (March 25, 2011)
ARIXTRA® Starter Kit patients regarding Triad Group’s alcohol prep products (January 24, 2011)

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Important Information for Betaseron® (interferon beta 1-b) Consumers Regarding Triad Group’s Alcohol Prep Products (January 20, 2011)
Bristol-Myers Squibb Recalls Coumadin (Warfarin Sodium) Crystalline 5 mg Tablets, Lot Number 9H49374A (May 02, 2011)

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Endo Pharmaceuticals Recalls Two Lots of Endocet (Oxycodone/Acetaminophen, USP) Tablets, 10 MG / 325 MG (June 24, 2011)
Important Information for Extavia® (interferon beta 1-b) Patients Regarding Triad Group's Alcohol Prep Products (January 10, 2011)

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Genentech Informs Customers Of Important Information About Triad Groups (January 13, 2011)
Greenstone Recalls Citalopram and Finasteride Due to Possible Mislabeling (March 26, 2011)

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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 24, 2011)
H and P Industries, Inc. Recall of All Lots of Povidine Iodine Prep Pads (March 15, 2011)

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McNeil Consumer Healthcare Announces Voluntary Recall Of One Product Lot Of TYLENOL ® Extra Strength Caplets 225 Count Distributed In The U.S. (June 28, 2011)
McNeil Consumer Healthcare Initiates Voluntary Recall Of Certain Over-The-Counter (OTC) Products (January 14, 2011)

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

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OTC DRUG Nationwide Recall--Important information for patients about IV PREP Antiseptic Wipes (March 05, 2011)
Ortho-McNeil Neurologics Voluntarily Recalls Two Lots of TOPAMAX® (April 14, 2011)
Ortho-McNeil-Janssen Pharmaceuticals, Inc. Voluntarily Recalls One Lot of RISPERDAL® Tablets and One Lot of Risperidone Tablets (June 17, 2011)

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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 26, 2011)

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Qualitest Pharmaceuticals Issues a Nationwide Voluntary Recall of Oral Contraceptives (September 15, 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)
Qualitest Pharmaceuticals Recalls Hydrocodone Bitartrate and Acetaminophen Tablets and Phenobarbital Tablets (February 05, 2011)

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Teva Pharmaceuticals, U.S.A issues a voluntary nationwide recall of Metronidazole Tablets USP, 250mg Due to Low Weight Tablets (January 06, 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 (January 05, 2011)

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Upsher-Smith Laboratories Announces Expansion of Voluntary Nationwide Recall. Affected Products Include Amantadine, Amlodipine, Androxy, Baclofen, Bethanechol, Jantoven® and Oxybutynin (February 18, 2011)
Upsher-Smith Laboratories Recalls Jantoven® Warfarin Sodium Tablets, USP, 3mg, Due To Mislabeled Bottles (February 16, 2011)

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

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Actavis Encourages Consumers to Return Fentanyl Transdermal System 25 mcg/h (November 04, 2010)
Actavis Inc. Issues a Voluntary Recall of 18 Lots of Fentanyl Transdermal System 25 mcg/h (October 21, 2010)
American Regent Initiates Nationwide Voluntary Recall of Sodium Bicarbonate Injection, USP 7.5% and 8.4%, 50mL Single Dose Vials Due to Particulate Matter (December 23, 2010)
American Regent Initiates Voluntary Recall of Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL, 30 mL Multiple Dose Vial (December 20, 2010)
Amgen Initiates Voluntary Nationwide Recall Of Certain Lots Of Epogen® And Procrit® (Epoetin Alfa) (September 24, 2010)

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Baxter Healthcare Corp. Initiates Voluntary Recall of HYLENEX (May 17, 2010)
Blacksmith Brands Announces Nationwide Voluntary Recall Of Four PediaCare Children's Products (May 28, 2010)
Bristol-Myers Squibb Initiates a Nationwide Voluntary Recall of Coumadin (R) 1 mg Tablet Blister Packs (July 12, 2010)

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Claris Lifesciences initiates a nationwide voluntary recall of all lots of Ciprofloxacin Inj. USP 200 mg / 100 mL, Ciprofloxacin Inj. USP 400 mg / 200 mL, Metronidazole Inj. USP 500 mg/100 ml and Ondansetron Inj., 32 mg / 50 mL. (June 01, 2010)
Cumberland Pharmaceuticals Announces Voluntary Recall of Acetadote® Vials (December 30, 2010)

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Hospira Announces an Expansion of a Nationwide Voluntary Recall of Certain Lots of Liposyn™ and Propofol That May Contain Particulate Matter (May 27, 2010)

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Johnson & Johnson Recall of Mylanta and Alternagel Liquid Products (November 29, 2010)
Johnson & Johnson Recall of Tylenol Cold Liquid Products (November 24, 2010)
Johnson & Johnson Recall of Children's BENADRYL® Allergy FASTMELT® Tablets and Junior Strength MOTRIN® Caplets (November 15, 2010)
Johnson & Johnson Recall of ROLAIDS® Extra Strength Softchews (November 15, 2010)

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Lundbeck Inc. Announces the Voluntary Nationwide Recall of Two Lots of NeoProfen® (ibuprofen lysine) Injection (July 30, 2010)

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McNeil Consumer Healthcare Announces Voluntary Recall Of All Lots Of Rolaids® Extra Strength Softchews, Roldaids® Extra Strength Plus Gas Softchews, And Roldaids® Multi-Symptom Plus Anti-Gas Softchews Sold In The United States (December 09, 2010)
McNeil Consumer Healthcare Announces Voluntary Recall of One Product Lot of TYLENOL® 8 Hour Caplets 50 Count Sold in The United States and Puerto Rico (October 18, 2010)
McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products (July 08, 2010)
Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab™ Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count (June 15, 2010)
McNeil Consumer Healthcare Announces Voluntary Recall of Certain OTC Infants’ and Children’s Products (April 30, 2010)
McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the Americas, UAE, and Fiji (January 15, 2010)
The Medicines Company Expands a Nationwide Recall for Certain Lots of Cleviprex® That May Contain Particulate Matter (March 17, 2010)

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P&G Voluntarily Recalls 4 Hour Decongestant Nasal Spray in the United States (June 24, 2010)
Pfizer To Recall One Lot Of Lipitor In The U.S. (December 22, 2010)
Pfizer Recalls Lipitor (40mg only) (October 09, 2010)
Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility (June 03, 2010)

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Reese Pharmaceutical Company Announces the Voluntary Nationwide Recall of Certain Over-The-Counter Cold Relief Products that are Mislabeled (December 09, 2010)
The Ritedose Corporation Announces the Voluntary Nationwide Recall of 0.083% Albuterol Sulfate Inhalation Solution, 3 mL Due to Mislabeled Unit Dose Vials (December 30, 2010)

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Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Ondansetron in 5% Dextrose Injection, 32 mg/50 mL Manufactured by Claris Lifesciences (June 02, 2010)
Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, USP 500 mg/100 mL (May 17, 2010)
Sandoz initiates voluntary recall in the US of all 50mg/2mL and 250mg/10mL vials of Methotrexate Injection, USP due to the presence of glass particulates (October 27, 2010)

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US Oftalmi Announces Voluntary Recall of the Camolyn Eye Drops Product Line, and Fisiolin Nasal Drops. Includes All Lots of 15mL Bottles (April 02, 2010)

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West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk (June 03, 2010)
WoStandard Homeopathic Company Voluntarily Recalls Hyland’s Teething Tablets (October 23, 2010)

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