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Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

No ongoing recalls currently shown

Based on the official records currently available to Public Health Trace, no recalls naming Akebia Therapeutics dba Keryx Biopharmaceutials, Inc are currently shown as ongoing. The 2 records below are historical recall records.

Public Health Trace has 2 recalls naming Akebia Therapeutics dba Keryx Biopharmaceutials, Inc as the recalling firm, republished from official FDA and USDA sources.

Recall history - 2 terminated records

Recalls by year

A bar chart of the number of recalls naming this company by year.

Recalls by year
YearRecalls
20201
20211
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FDA Recall TerminatedTerminated: February 10, 2022Historical recordClass III

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.

by Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Reason
Failed Dissolution Specifications
Published
February 24, 2021
Distribution
Nationwide

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FDA Recall TerminatedTerminated: September 1, 2021Historical recordClass II

Auryxia (ferric citrate) tablets, 210 mg, 200-count bottles, Rx only, Manufactured for and distributed by: KERYX BIOPHARMACEUTICALS, INC., One Marina Park Drive, 12th Floor, Boston, MA 02210, NDC 59922-631-01

by Akebia Therapeutics dba Keryx Biopharmaceutials, Inc

Reason
CGMP Deviations
Published
December 30, 2020
Distribution
Nationwide

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Showing 1–2 of 2 results

Some FDA recall records on this page come from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

This page lists recalls that name Akebia Therapeutics dba Keryx Biopharmaceutials, Inc as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.