Share:
News
February 4, 2011
American Regent Recalls One Lot of Sodium Thiosulfate Injection Due to Particulates
American Regent is recalling One Lot of Sodium Thiosulfate Injection, USP, 10% (100 mg/mL), 10 mL Single Dose Vial due to particulate contamination.
February 4, 2011
FDA Announces Upcoming Shortage of Vetsulin for Dogs and Cats in the Critical Need Program
The Food and Drug Administration (FDA) announced today an anticipated shortage of Vetsulin (porcine insulin zinc suspension), a product used to treat diabetes mellitus in dogs and cats. Vetsulin is manufactured by Intervet/Schering-Plough Animal Health and is only available to animals currently enrolled in the Vetsulin Critical Need Program.
January 31, 2011
Family Farm Complete Horse 10 Horse Feed Recalled Due to Possible Monensin Sodium Contamination
Manna Pro Products, LLC is voluntarily recalling a single lot (1006) of Family Farm Complete Horse 10 horse feed, UPC 0 95668 90151 6, packaged in 40 lb. bags because it may contain monensin sodium (Rumensin). Monensin sodium is a medication approved for use in some livestock and poultry species, but can be fatal to horses if fed at sufficiently high levels.
January 28, 2011
Merrick Pet Care Recalls Jr. Texas Taffy Pet Treats Due to Potential Salmonella Contamination
Merrick Pet Care, Inc. of Amarillo, Texas is recalling the Jr. Texas Taffy pet treat (ITEM # 27077, UPC # 02280827077, All Lots up to and including 10364) because they have the potential to be contaminated with Salmonella.
January 6, 2011
Teva Pharmaceuticals Recalls One Lot of Metronidazole 250mg Tablets
Teva Pharmaceuticals is recalling Metronidazole Tablets USP, 250mg, lot 312566, expiration date 05/2012. This product lot is being recalled due to the presence of underweight tablets.
December 30, 2010
American Regent Recalls Sodium Bicarbonate Injection, USP 7.5% and 8.4%, 50mL Single Dose Vials Due to Particulate Matter
American Regent is conducting a nationwide voluntary recall to the consumer and user level of ALL unexpired lots of the following products: Sodium Bicarbonate Injection, USP, 7.5%, 44.6 mEq/50 mL, Single Dose Vial NDC # 0517-0639-25 and Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq/50 mL, Single Dose Vial NDC # 0517-1550-25.
December 30, 2010
American Regent Recalls of Dexamethasone Sodium Phosphate Injection, USP 4 mg/mL, 30 mL Multiple Dose Vial
American Regent is conducting a nationwide voluntary recall of the following: Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 30 mL Multiple Dose Vial, NDC # 0517-4930-25.
October 29, 2010
B. Braun Recalls 7 Lots of Heparin Injection Due to Contamination
B. Braun is recalling seven lots of heparin injection products. Testing of retained crude heparin samples indicated a trace amount of oversulfated chondroitin sulfate (OSCS) contaminant.
