Class III · Low risk
FUROSEMIDE Tablets USP
CGMP Deviations: The active pharmaceutical ingredient (API) intended for use in furosemide oral solution USP was inadvertently used to manufacture the recalled furosemide tablets USP.
5 recalls · Class III, newest first
CGMP Deviations: The active pharmaceutical ingredient (API) intended for use in furosemide oral solution USP was inadvertently used to manufacture the recalled furosemide tablets USP.
CGMP Deviations: The active pharmaceutical ingredient (API) intended for use in furosemide oral solution USP was inadvertently used to manufacture the recalled furosemide tablets USP.
CGMP Deviations: Confirmed customer compliant of odor when turning on a cylinder of medical air.
CGMP Deviations: Confirmed customer compliant of odor when turning on a cylinder of medical air.
CGMP Deviations: Product excipient was not re-tested at the appropriate date.