Drug Recalls

256 total items found
Displaying page 1 of 6       1   2   3   4    

Baxter Initiates U.S. Voluntary Recall of One Lot of Peritoneal Dialysis Solution Due to Container-Closure Non-Integrity

Recall Date: Wednesday, March 5th, 2014

---

Agila Specialties Private Limited Initiates Voluntary Nationwide Recall of 10 Lots of Etomidate Injection 2 mg/mL - 10 mL and 20 mL due to the Presence of Particulate Matter and/or Illegible and Missing Lot Number and/or Expiry Date

Recall Date: Wednesday, February 19th, 2014

---

Ben Venue Laboratories, Inc. Issues A Voluntary Nationwide Patient Level Recall Of Acetylcysteine Solution 10%, Usp, Lot 2005479

Recall Date: Friday, February 14th, 2014

---

Tandem Diabetes Care Expands Voluntary Recall for Select Lots of Insulin Cartridges Used with t:slim Insulin Pump

Recall Date: Wednesday, February 12th, 2014

---

Stemvida International Corporation Recalls StemAlive 90 Capsules Containing Undeclared Milk

Recall Date: Friday, January 17th, 2014

---

Human Science Foundation Issues Voluntary Nationwide Recall of Pro ArthMax Due to Undeclared Active Pharmaceutical Ingredients

Recall Date: Tuesday, January 14th, 2014

---

Tandem Diabetes Care Initiates Voluntary Recall for Specific Lots of Insulin Cartridges Used with t:slim Insulin Pump

Recall Date: Tuesday, January 14th, 2014

---

Baxter Initiates Nationwide Voluntary recall Of Select Lots of Premix Parenteral Nutrition

Recall Date: Friday, January 3rd, 2014

---

Baxter Initiates Worldwide Voluntary Recall Of Select Lots Of 5 percent Dextrose Injection, USP And 0.9 percent Sodium Chloride Injection, USP Intravenous (IV) Solutions

Recall Date: Thursday, December 26th, 2013

---

Hospira Issues a Voluntary Nationwide Recall of One Lot of Lidocaine HCl Injection, USP, 2%, 5 Ml in 5 Ml Vial, Due to Presence of Particulate Matter

Recall Date: Monday, December 23rd, 2013

---

Alexion Provides Update on Previously Communicated November 2013 Voluntary Nationwide Recall of Two Lots of Soliris (eculizumab) Concentrated Solution for Intravenous Infusion

Recall Date: Friday, December 13th, 2013

---

Baxter Initiates Nationwide Voluntary Recall of One Lot of Nitroglycerin in 5% Dextrose Injection

Recall Date: Wednesday, November 27th, 2013

---

Deseo Rebajar Inc. Issues Voluntary Puerto Rico Recall of Adipotrim XT Due to Underclared Fluoxetine

Recall Date: Thursday, November 21st, 2013

---

Perrigo Initiates Nationwide Voluntary Product Recall of Acetaminophen Infant Suspension Liquid, 160 mg/5 mL, Due to a Potential Defect with the Co-packaged Oral Syringe

Recall Date: Friday, November 1st, 2013

---

Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.25% Marcaine™ (Bupivacaine HCL Injection, USP), 75mg/30ml, Single-Dose - Preservative Free Vial Due to Presence of Particulate Matter

Recall Date: Friday, October 18th, 2013

---

Nephron Pharmaceuticals Corporation Announces Voluntary Recall of Albuterol Sulfate Inhalation Solution, 0.083%

Recall Date: Thursday, October 17th, 2013

---

B. Braun Medical Inc. Issues Voluntary Nationwide Recall of Lot H3A744, 1 gram Cefepime for Injection USP and Dextrose Injection USP Due to Visible Particulate Matter

Recall Date: Tuesday, October 15th, 2013

---

H&H Medical Corporation Issues Nationwide Recall of Emergency Cricothyrotomy Kit

Recall Date: Friday, October 4th, 2013

---

Hospira Issues A Voluntary Nationwide Recall Of One Lot Of 1% Lidocaine HCL Injection Due To The Presence Of Dark Particulate

Recall Date: Friday, October 4th, 2013

---

HOSPIRA ISSUES A VOLUNTARY NATIONWIDE RECALL OF ONE LOT OF METOCLOPRAMIDE INJECTION, USP, AND TWO LOTS OF ONDANSETRON INJECTION, USP, DUE TO GLASS (GLASS STRANDS) PARTICULATES CAUSED BY GLASS SUPPLIER DEFECT

Recall Date: Wednesday, October 2nd, 2013

---

Haute Health, LLC Conducts Voluntary Nationwide Recall of All Lots Of Virilis Pro, PHUK And Prolifta Capsules Due To Undeclared Ingredients

Recall Date: Monday, September 30th, 2013

---

Baxter Initiates Voluntary Recall of Two Lots of Dual Luer Lock Caps

Recall Date: Thursday, September 19th, 2013

---

HeartSine Technologies, Ltd. Issues Global Correction of Samaritan® 300/300P PAD

Recall Date: Monday, September 16th, 2013

---

Hospira Issues a Voluntary Nationwide Recall of One Lot of 0.25% Bupivacaine HCL Injection, USP (2.5 MG/ML), 30 ML Single-Dose Vial and One Lot of 0.75% Bupivacaine HCL Injection, USP (7.5 MG/ML), 30 ML Single Dose Vial Due to Presence of Particulate Matter

Recall Date: Friday, September 13th, 2013

---

Park Compounding: Sterile Medication Recall - Concerns of Sterility Assurance at Testing Vendor

Recall Date: Tuesday, September 10th, 2013

---

Avella Specialty Pharmacy Issues Voluntary Nationwide Recall of Two Medications Due to Concerns of Sterility Assurance at Testing Vendor

Recall Date: Monday, September 9th, 2013

---

University Compounding Pharmacy Initiates a Nationwide Voluntary Recall of Certain Pharmacy Products due to Lack of Assurance of Sterility Concerns

Recall Date: Friday, September 6th, 2013

---

Altaire Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of 9 Lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution Sold Under Several Brands Because the Preservative May Not Be Effective Through Expiry

Recall Date: Friday, September 6th, 2013

---

Hospira Issues A Voluntary Nationwide Recall Of One Lot Of Aminosyn II 10 percent, Sulfite-Free, Due To Foreign Particulate Matter

Recall Date: Friday, August 30th, 2013

---

Cubist Pharmaceuticals Issues Voluntary Nationwide Recall of Four Lots of Cubicin (Daptomycin for Injection) 500mg in 10ml Single Use Vials Due to Presence of Particulate Matter

Recall Date: Thursday, August 29th, 2013

---

Wellness Pharmacy, Inc. Issues Nationwide Voluntary Recall of Certain Sterile Products due to Laboratory Results Indicating Microbial Contamination

Recall Date: Tuesday, August 27th, 2013

---

JCB Laboratories Issues Voluntary Recall of Six Drug Product Lots Due to Concerns of Sterility Assurance at Testing Vendor

Recall Date: Tuesday, August 27th, 2013

---

Park Pharmacy & Compounding Center is Issuing a Voluntary Recall of Two Compounded Sterile Preparations. The Recall is Due to a Lack of Sterility Assurance

Recall Date: Monday, August 26th, 2013

---

Covidien Initiates a Voluntary Recall of Certain Lots of Monoject Prefill Flush Syringes Sold in the United States and Bermuda

Recall Date: Monday, August 19th, 2013

---

Hospira Issues Important Safety Information for Blood Sets

Recall Date: Tuesday, August 13th, 2013

---

Specialty Compounding, LLC Issues Nationwide Voluntary Recall of All Lots of Unexpired Sterile Products Due to Reports of Adverse Events

Recall Date: Saturday, August 10th, 2013

---

Health and Beyond LLC Issues Voluntary Nationwide Recall of Tranquility Product Due to Product Having Traces of Pharmaceutical Ingredients

Recall Date: Wednesday, August 7th, 2013

---

Bethel Nutritional Consulting, Inc. Expands Voluntary Recall to Include Bethel Advance and Quick Thin Products Found to Contain an Undeclared Drug Ingredient

Recall Date: Monday, August 5th, 2013

---

Nexus Pharmaceuticals Inc. Issues Voluntary Nationwide Recall of Benztropine Mesylate Injection, USP 2 mg/2 mL (1 mg/mL), in 2 mL Single Dose Vials

Recall Date: Friday, August 2nd, 2013

---

Beacon Hill Pharmacy d/b/a Rxtra Solutions Issues Voluntary Nationwide Recall of Certain Sterile Products Due to a Question of Sterility Assurance

Recall Date: Thursday, August 1st, 2013

---

Hardmenstore.com Issues Voluntary Nationwide Recall of Silver Sword and Clalis at the Request of the FDA

Recall Date: Monday, July 15th, 2013

---

Fresenius Kabi USA Issues Voluntary Nationwide Recall of Benztropine Mesylate Injection, USP 2 mg/2 mL (1 mg/mL), in 2 mL Single Dose Vials

Recall Date: Monday, July 1st, 2013

---

Advance Pharmaceutical Inc. Issues Voluntary Recall of One Lot of Enteric Coated Aspirin Tablets, 81 mg, Due to Health Risk

Recall Date: Wednesday, June 19th, 2013

---

Sagent Pharmaceuticals Expands a Nationwide Voluntary Recall to All Lots of Vecuronium Bromide for Injection, 10mg Single Use Vials Manufactured by Mustafa Nevzat (MN Pharmaceuticals)

Recall Date: Thursday, June 13th, 2013

---

Zydus Pharmaceuticals USA Inc. Issues Voluntary Nationwide Recall of Warfarin 2 mg Tablets, Lot MM5767, Expiration Date June 2014, Due to Oversized Tablets

Recall Date: Wednesday, June 12th, 2013

---

Sagent Pharmaceuticals Initiates a Nationwide Voluntary Recall of Three Lots of Vecuronium Bromide for Injection, 10mg Manufactured by Mustafa Nevzat (MN Pharmaceuticals) Due to Elevated Impurity Levels

Recall Date: Monday, June 10th, 2013

---

Fresenius Kabi USA Initiates Voluntary Recall of Single Lot of Magnesium Sulfate

Recall Date: Wednesday, May 29th, 2013

---

Lowlite Investments, Inc. d/b/a Olympia Pharmacy Announces a Voluntary Multi-State Recall of All Sterile Compounded Products Compounded Between December 17, 2012, and March 27, 2013, Due to Concerns About Sterility Assurance

Recall Date: Wednesday, May 29th, 2013

---

Main Street Family Pharmacy, LLC Issues Voluntary Nationwide Recall of All Sterile Compounded Products

Recall Date: Tuesday, May 28th, 2013

---

Sandoz US Announces Voluntary Nationwide Recall of two lots of Methotrexate Sodium, USP, Injectable Vials, 25mg/mL, 40mL vials

Recall Date: Monday, May 20th, 2013

256 total items found
Displaying page 1 of 6       1   2   3   4