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Risk Managers and Pharmacy healthcare personnel are informed by the FDA that certain Hospira Injectable Drug Products are recalled because of visible particles embedded in the glass located at the neck of the vial which can cause adverse events. Background of Hospira Injectable Drug Products Certain injectable drug products, by Hospira, Inc, are used to [...]

The US FDA informs Consumers and Pharmacy Healthcare Personnel that Infants’ Tylenol Oral Suspension, 1 oz. Grape is recalled because consumers reported complaints with SimpleMeasure dosing system. Background of Infants’ Tylenol Oral Suspension, 1 oz. Grape Infants’ Tylenol Oral Suspension, 1 oz. Grape, by McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is an OTC (over-the-counter) [...]

Consumers are informed by the FDA that Nidek Medical Products, Inc., Mark 5 Nuvo, Nuvo 8 and Nuvo Lite Oxygen Concentrators are recalled because capacitor failure can result in fire hazard and loss of supplemental oxygen causing serious adverse health consequences, including death. Background of Mark 5 Nuvo, Nuvo 8 and Nuvo Lite Oxygen Concentrators [...]

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, [...]