Safety Alerts & Recalls

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Recall on Several Lots of Dextroamphetamine 10 mg Tablets
The ETHEX Corporation has voluntarily recalled several lots of DEXTROAMPHETAMINE 10 mg tablets. These tablets may be oversized and contain more drug than appropriate. This could result in patients receiving as much as twice the expected dosage of this drug. The lot numbers involved in the recall are: Dextroamphetamine Sulfate Tablets, 10 mg: Lots: 73934, 75892, 77945, 81137, 86320 with expiration dates ranging from June 2009 to May 2011 For more information, please visit: http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2008/ucm112519.htm
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Recall on Several Lots of Morphine Sulfate Extended Release and Immediate Release Tablets
The ETHEX Corporation has voluntarily recalled several lots of MORPHINE SULFATE EXTENDED RELEASE 15 mg and MORPHINE SULFATE IMMEDIATE RELEASE 15 mg and 30 mg tablets. These tablets may be oversized and contain more drug than appropriate. This could result in patients receiving as much as twice the expected dosage of this drug. The lot numbers involved in the recall are: Morphine Sulfate Extended Release Tablets, 15 mg: Lots: 81175, 82514-16, 89660, 89664, 89667, 90249-51, and 91687 with expiration dates ranging from December 2008 to February 2010 Morphine Sulfate Immediate Release Tablets, 15 mg: Lots: 77852-54, 81746, 82519-20, 84113, and 90276-78 with expiration dates ranging from September 2009 to January 2011 Morphine Sulfate Immediate Release Tablets, 30 mg: Lots: 75093, 77855-57, 82297, 82521-22, 87239, 88925, and 90288-98 with expiration dates ranging from August 2009 to March 2011 For more information, please visit: http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm110547.htm
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Date Published Title Drug Source
2008-11-10 Recall on Several Lots of Dextroamphetamine 10 mg Tablets Dextroamphetamine Manufacturer
2008-11-10 Recall on Several Lots of Morphine Sulfate Extended Release and Immediate Release Tablets Morphine Manufacturer
2008-11-10 Recall on Several Lots of Isosorbide Mononitrate Extended Release 30 mg and 60 mg Tablets Isosorbide Manufacturer
2008-11-06 Recall of Single Lot of PREMPRO 0.3 mg/1.5 mg EZ-DIAL Dispensers Estrogens Conjugated with Medroxyprogesterone FDA
2008-11-06 Recall of Single Lot of ReliOn Syringes Insulin FDA
2008-11-06 Recall of Single Lot of ReliOn Syringes Insulin Aspart FDA
2008-11-06 Recall of Single Lot of ReliOn Syringes Insulin Glargine FDA
2008-11-06 Recall of Two Lots of Lisinopril 10 mg Lisinopril FDA
2008-11-05 Generic Manufacturer Recalls Single Lot of BACITRACIN Bacitracin FDA
2008-11-05 Generic Manufacturer Recalls Several Lots of Hemorrhoidal HC 25 mg Suppositories Hydrocortisone FDA
2008-10-17 Raptiva (Efalizumab) Boxed Warning Efalizumab FDA
2008-10-16 Selected Recall of ETHEX Dextroamphetamine Sulfate 5 mg Tablets Dextroamphetamine Manufacturer
2008-10-10 Important Information About Safe Use of Children's Cough and Cold Medicine Chlorpheniramine Manufacturer
2008-10-10 Important Information About Safe Use of Children's Cough and Cold Medicine Manufacturer
2008-10-10 Important Information About Safe Use of Children's Cough and Cold Medicine Dextromethorphan Manufacturer
2008-10-10 Important Information About Safe Use of Children's Cough and Cold Medicine Guaifenesin Manufacturer
2008-10-10 Important Information About Safe Use of Children's Cough and Cold Medicine Phenylephrine Manufacturer
2008-10-08 Early Communication About Ongoing Safety Review of Spiriva Tiotropium FDA
2008-10-08 Important Information About Safe Use of Children's Cough and Cold Medicine Acetaminophen Manufacturer
2008-10-03 First Reported Case of Progressive Multifocal Leukoencephalopathy (PML) in a Raptiva Patient Efalizumab Manufacturer