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Risk Managers and Pharmacists are informed by the US FDA that Hospira, Inc., Hydromorphone Hydrochloride Injection 2 MG/ML, 1 mL fill in 2.5 mL Carpuject is recalled because it may contain more than the intended fill volume resulting in respiratory depression and reduced heart rate including circulatory collapse. Background of Hydromorphone Hydrochloride 2 MG/ML, 1 [...]

FDA issued a Class 1 recall of Naturalyte and Granuflo Acid Concentrate because inappropriate prescription of these products can contribute to metabolic alkalosis leading to serious adverse events, including death. Background of Naturalyte and Granuflo Acid Concentrate The Naturalyte and Granuflo Dry Acid Concentrate, by Fresenius Medical Care North America, are used during hemodialysis for [...]

The US FDA informs Risk Managers and consumers that Hospira, Inc, Hydromorphone Hydrochloride Injection 1 MG/ML, (C-II) 1 ML Fill in 2.5 ML Carpuject is recalled because it may contain more than the intended fill volume resulting in respiratory depression and reduced heart rate including circulatory collapse. Background of Hydromorphone Hydrochloride Injection 1 MG/ML, (C-II) [...]

Risk Manager and Pain Management healthcare personnel are informed by the FDA that Hospira, Inc, Morphine Sulfate Injection USP, 4 mg/mL (C-II), 1 mL fill in 2.5 mL Carpuject is recalled because it may contain more than the intended fill volume resulting in respiratory depression and low blood pressure. Background of Morphine Sulfate Injection USP, [...]