The U.S. Food and Drug Administration is alerting health care professionals and consumers of a voluntary recall of all non-expired drug products produced for sterile use by Unique Pharmaceuticals Ltd., of Temple, Texas.
FDA approves Zydelig for three types of blood cancers
The U.S. Food and Drug Administration today approved Zydelig (idelalisib) to treat patients with three types of blood cancers.
American Health Packaging Announces the Voluntary Nationwide Recall of Ibuprofen Tablets, USP, 600 mg, 100 Hospital Unit Dose and Oxcarbazepine Tablets, 300 mg, 100 Hospital Unit Dose
American Health Packaging (Columbus, OH) has voluntarily recalled Lot #142588, Expiration Date, 01/2016 of Ibuprofen Tablets, USP, 600 mg, in a hospital unit dose presentation that may contain individual blistered doses labeled as Oxcarbazepine Tablets, 300 mg, lot #142544.
Wegmans Issues Voluntary Recall of Bakery Products That May Contain Fresh Peaches, Nectarines and Plums Supplied by Wawona Packing Company
Wegmans Food Markets, Inc. is voluntarily recalling several in-store baked desserts that may contain fresh peaches, nectarines, and/or plums. The fruit was supplied by California-based Wawona Packing Company, which issued a voluntary recall when routine testing by the company showed potential contamination with Listeria monocytogenes.
Wawona Packing Co. Takes Precautionary Step of Voluntarily Recalling Fresh, Whole Peaches, Plums, Nectarines, and Pluots Because of Possible Health Risk
Wawona Packing Company of Cutler, Calif is voluntarily recalling certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 1, 2014 through July 12,2014 due to the potential of the products being contaminated with Listeria monocytogenes. Wawona Packing has notified retailers of the specific lots being recalled.
Whole Foods Market Hyannis Recalls Chocolate Chewies Cookies Due to Undeclared Tree Nut Allergen
Whole Foods Market is recalling ‘Chocolate Chewies’ produced and sold in the Hyannis, Massachusetts location due to an undeclared tree nut allergen. The product was sold in the store between Sunday, July 13, 2014 and Friday, July 18, 2014 in clear, clamshell packaging and has a Use By date of: 7/18/14.
Unique Pharmaceuticals, Ltd. Announces a Voluntary Nationwide Recall of all Sterile Compounded Preparations Within Their Expiry Period Due to a Lack of Sterility Assurance
Unique Pharmaceuticals, Ltd., (“Unique� or “the Company�) today announced a voluntary nationwide recall of all sterile drug preparations compounded by the outsourcing facility that have not reached the expiration date listed on the products. Unique is initiating the recall due to FDA’s concerns associated with Unique’s compounding facilities and compounding processes that FDA contends present a lack of sterility assurance and were observed during recent FDA inspections.
Indictment of FedEx Corporation for Illegally Distributing Prescription Drugs
The U.S. Attorney for the Northern District of California today charged the FedEx Corporation with conspiring with two separate but related online pharmacy organizations to distribute controlled substances and prescription drugs to U.S. consumers without requiring their customers to have a valid prescription, as required by the Federal Food, Drug, and Cosmetic Act.
Mars Food North America Voluntarily Recalls Specific Batch and Item Number Representing Less Than 2,000 Cases
Mars Food North America is voluntarily recalling two Lot Codes of UNCLE BEN’S® READY RICE® Garden Vegetable with Peas, Carrots & Corn pouch product, representing less than 2,000 cases. Some pouches in these lot codes were filled with a different product that contains barley, a non-wheat source of gluten, which is not declared on the product packaging.
FDA approves new product to treat rare genetic disease
The U.S. Food and Drug Administration yesterday approved Ruconest, the first recombinant C1-Esterase Inhibitor product for the treatment of acute attacks in adult and adolescent patients with hereditary angioedema (HAE).