FDAJanuary 29, 2021drug
Auryxia (ferric citrate) tablets, 210 mg*, 200 tablets bottle, RX ONLY, Manufactured for and distributed by: KERYX BIOPHARMACEUTICALS, INC., 245 First Street, Suite 1400, Cambridge, MA 02142, USA, NDC 59922-0631-01.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Failed Dissolution Specifications
What to do
FDA enforcement status: Terminated
Brands named
akebia therapeutics dba keryx biopharmaceutialsakebiaakebia therapeutics
UPCs
59922063101
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- CPSCLiKee Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by ChilanTech2026-06-11
- CPSCResistance Bands Recalled Due to Serious Injury from Impact Hazard; Imported by HomeProGym2026-05-21
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