RecallDepth
Class III Terminated

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.

This recall has been terminated (originally issued February 24, 2021).

Company
Akebia Therapeutics Dba Keryx Biopharmaceutials, Inc
Recall Initiated
January 29, 2021
Posted
February 24, 2021
Recall Number
D-0260-2021
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
17,664 bottles
Firm Location
Cambridge, MA, United States
Official Source
View on FDA website ↗

Reason for Recall

Failed Dissolution Specifications

Distribution

Nationwide.

Lot / Code Info

Lots #: CDKSN, CDPPH, Exp January 2022; Lot #: CDPPK, Exp February 2022.

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