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Chronic Kidney Disease Drug Recalled
The recall affects 200-count bottles of 210-mg Auryxia tablets (NDC 59922-0631-01) from lots CDKSN (Exp. 1/22), CDPPH (Exp. 1/22), and CDPPK (Exp. 2/22). The tablets were distributed throughout the United States.
Akebia Therapeutics, which does business as Keryx Biopharmaceuticals, voluntarily initiated the recall January 29, 2021. The FDA designated the recall Class III on February 17, 2021, suggesting use of the recalled tablets is not likely to cause harm.
Auryxia is a prescription medication used to control serum phosphorus levels of adults with chronic kidney disease on dialysis and to treat iron deficiency anemia in adults with chronic kidney disease not on dialysis.
—Jolynn Tumolo