Hospira, Inc.(NYSE: HSP), announced today it has initiated a voluntary nationwide recall of one lot of 1% Lidocaine HCI Injection, USP, 10 mg/mL, 20 mL Multiple-dose Fliptop Vial, NDC 0409-4276-01 Lot 25-090-DK (the lot number may be followed by 01 or 02).
H&H Medical Corporation Issues Nationwide Recall of Emergency Cricothyrotomy Kit
On August 27, 2013, H&H Medical Corporation initiated a nationwide recall of 6,619 units of the H&H Emergency Cricothyrotomy Kit. The product has been found to show the potential for a defective cuff balloon on the provided endotracheal airway.
FDA approves Clinolipid for intravenous nutrition
The U.S. Food and Drug Administration today approved Clinolipid (lipid injectable emulsion, USP) for intravenous feeding (parenteral nutrition) in adult patients, providing a source of calories and essential fatty acids for adult patients who are unable to eat or drink.
OnTime Distribution Inc. Recalls PRAN brand Spice Powder TURMERIC Due To Excessive Levels of Lead
OnTime Distribution Inc. of Brooklyn, NY, is voluntarily recalling PRAN brand Spice Powder TURMERIC because it was found to contain high levels of lead that could cause health problems to consumers, particularly infants, small children, and pregnant women if consumed. Recent analysis of the product found that it contained lead levels as high as 28 and 42 parts per million (ppm).
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
Hospira, Inc. (NYSE: HSP), announced today it initiated a voluntary nationwide recall of one lot of Metoclopramide Injection, USP, 10 mg/2 mL (5 mg/mL), NDC 0409-3414-01, Lot 28-104-DK and two lots of Ondansetron Injection, USP, 4 mg/2 mL, (2 mg/mL), NDC 0409-4755-03, Lots 29-484-DK and 29-510-DK. This action is due to a confirmed vial defect where glass particulate matter (glass strands) were identified as being affixed to the inside of the vial walls. There is potential for the glass particulates to dislodge into the solution.
Mandy Star Trading Inc. Is Issuing an Alert on Undeclared Sulfites in "Good Taste" Brand Plum
Mandy Star Trading Inc., located at 349 Maujer Street Brooklyn NY 11206 is recalling “Good Taste” brand Plum, because it contains undeclared sulfites and unallowed E124 (Acid Red 18) dye. People who have a severe sensitivity to sulfites run the risk of serious or life-threatening allergic-like reactions if they consume this product.
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FDA approves new drug to treat major depressive disorder
The U.S. Food and Drug Administration today approved Brintellix (vortioxetine) to treat adults with major depressive disorder.
Big Blue Fisheries, Llc Recalls All Smoked Products From All Lots, Various Sizes, in Vacuum Packaging Because of Possible Health Risk
Big Blue Fisheries is recalling ALL smoked products from all lots and codes, various sizes, in vacuum packages because the products may not have been properly cooked and have the potential to be contaminated with Clostridium botulinum, a bacterium which can cause life-threatening illness or death. Consumers are warned not to use the product even if it does not look or smell spoiled.
Carefusion Provides Update On Voluntary Recall Of Avea® Ventilator
CareFusion issued the following update regarding its previously announced voluntary recall of AVEA® ventilators. The company initiated the voluntary recall on Sept. 3, 2013.
Haute Health, LLC Conducts Voluntary Nationwide Recall of All Lots Of Virilis Pro, PHUK And Prolifta Capsules Due To Undeclared Ingredients
Haute Health, LLC is voluntarily recalling all lots of Virilis Pro, PHUK and Prolifta at the retail and consumer level. Virilis Pro, PHUK and Prolifta have been found to contain amounts of the PDE-5 Inhibitor sildenafil, which is an active ingredient in an FDA-approved drug for erectile dysfunction (ED).