09.14.18
Urgent: Dr. Reddy’s Laboratories issues a voluntary recall for 20 lots of Zoledronic Acid Injection, 5 mg/100 mL
Dr. Reddy’s Laboratories Inc., is issuing a voluntary product recall for Zoledronic Acid Injection, 5 mg/100 mL. The affected lots are listed below for the lots distributed from February 21, 2017 to June 15, 2018. 
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07.31.18  Urgent: Akorn Inc. issues a voluntary recall for 1 lot of Lidocaine 2.5% and Prilocaine Cream, 2.5%
Akorn Inc., is issuing a voluntary product recall for Lidocaine 2.5% and Prilocaine Cream, 2.5%®. The affected lots are listed below. T
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07.18.18  Sandoz issues a voluntary recall for all lots of Ondansetron Orally Disintegrating Tablets (ODT) and Risperidone Orally Disintegrating Tablets (ODT)
Sanoz Inc. is voluntarily implementing a U.S. Consumer Product Safety Commission (“CPSC”)-approved corrective action plan for blister packs of Sandoz Ondansetron Orally Disintegrating Tablets (ODT) in 4 mg and 8 mg dosage strengths and Risperidone Orally Disintegrating Tablets (ODT) in 0.5 mg, 1 mg, 2 mg, 3 mg and 4 mg dosage strengths.
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06.12.18  URGENT: Grifols issues a voluntary recall for 1 lot of Profilnine
Grifols Biologicals is initiating a voluntary product recall of one lot of Profilnine.
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06.11.18  Update: NIOSH Product Shipping
Updated packing method for hazardous or potentially hazardous drugs goes into effect on ASD Healthcare orders placed today, Monday, June 11, 2018. 
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05.10.18  URGENT: Bracco issues voluntary recall 05/18
Bracco is conducting a voluntary recall for one lot of E-Z-PASTE® Barium Sulfate Esophageal Cream (60% w/w) due to an out of specification result for a preservative assay, methylparaben, during stability testing on one lot of E-Z-PASTE®.
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