The FDA is recommending healthcare professionals not use any products by the New England Compounding Center in Framingham, Mass., due to potentially contaminated medication causing a fungal meningitis outbreak, according to the American Society of Anesthesiologists.
The FDA has linked a fungal meningitis outbreak to potentially contaminated methylprednisolone acetate from NECC, though the exact source of the outbreak is still ongoing.
However, the FDA has observed fungal contamination from a sealed vial of the injectable steroid produced and distributed by NECC and is conducting additional testing to confirm the exact species of fungus.
As a precaution, governmental officials recommend discontinuing use of all NECC products while retaining and securing all remaining products purchased from NECC until the FDA provides instructions on disposal.
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The FDA has linked a fungal meningitis outbreak to potentially contaminated methylprednisolone acetate from NECC, though the exact source of the outbreak is still ongoing.
However, the FDA has observed fungal contamination from a sealed vial of the injectable steroid produced and distributed by NECC and is conducting additional testing to confirm the exact species of fungus.
As a precaution, governmental officials recommend discontinuing use of all NECC products while retaining and securing all remaining products purchased from NECC until the FDA provides instructions on disposal.
More Articles on Anesthesia:
Somnia Anesthesia to Offer Webinar on Anesthesia Career Trends
CBIZ Acquires Anesthesia Billing Company ProMedical
Physician Lawmakers Concerned by Policy to Allow Patients to Report Medical Mistakes