American Regent is conducting a nationwide voluntary recall to the Retail/Hospital level of the following product: Epinephrine Injection, USP, 1:1000, 1 mL Ampules NDC #0517-1071-25 Lot #1395, Exp Date: July 2012 Read more »
American Regent Initiates Nationwide Voluntary Recall of Cyanocobalamin Injection, USP, 100 mcg/mL, 1ml Vial Lot #s 1662, 1679, 1683 Due to Cracks in…
American Regent is conducting a nationwide voluntary recall to the Retail/Hospital level of the following product: Cyanocobalamin Injection, USP, 100 mcg/mL, 1 mL Vial NDC # 0517-0031-25 Lot # 1662, Exp Date: November, 2013, Lot # 1679, Exp Date: November, 2013, Lot # 1683, Exp Date: November, 2013. Read more »
American Regent, Inc. Initiates Voluntary Recall of Seventeen Lots of Vasopressin Injection, USP, Multiple Dose Vials due to Sub-Potency
American Regent, Inc. is conducting a nationwide voluntary recall of 5 lots of Vasopressin Injection, USP 20 units/mL (200 units/10mL), 10 mL Multiple Dose Vials; 11 lots of Vasopressin Injection, USP 20 units/mL, 1 mL Multiple Dose Vials; and 1 lot of Vasopressin Injection, USP 10 units/0.5 mL,0.5 mL Multiple Dose Vials to the Retail/Hospital level. Read more »
Bedford Laboratories™ Statement Regarding Nationwide Voluntary Recall Of One Lot Of Indomethacin For Injection, USP 1 MG Single Dose Vial
On April 19, 2011, Bedford Laboratories™, a division of Ben Venue Laboratories, Inc., initiated a nationwide voluntary recall of the following product: PLEASE NOTE: This recall is for Lot 1948138 Only. Read more »
American Regent Initiates Voluntary Nationwide Recall of Bacteriostatic Sodium Chloride Injection, USP, 0.9% 30 mL Multiple Dose Vials
American Regent is conducting a nationwide voluntary recall of the three lots listed below of the following product: Bacteriostatic Sodium Chloride Injection, USP, 0.9%, 30 mL, Multiple Dose Vials NDC # 0517-0648-25 Read more »
American Regent Initiates Voluntary Recall 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. PLEASE NOTE: This recall, initiated on December 20, 2010 to the User Level, is for these lots only. Read more »
Natural Wellness, Inc. Issues a Nationwide Voluntary Recall of Masxtreme Capsules, Marketed as a Dietary Supplement – 08/24/10
Natural Wellness is announcing that it is conducting a nationwide voluntary recall of MasXtreme, Lot # 907043, UPC 094922300805. Laboratory analysis conducted by FDA has determined the product contains undeclared amounts of Aminotadalafil, an analog of tadalafil... Read more »
