Keryx Biopharmaceuticals, Inc.

FDA Regulatory Profile

Keryx Biopharmaceuticals, Inc. appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1389-2020, Class II) was initiated on July 10, 2020.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1389-2020Class IIAuryxia (ferric citrate) tablets 210 mg, Rx Only, 200 tablets per bottle, Manufactured for and distrJuly 10, 2020
D-0133-2018Class IIIAuryxia (ferric citrate) tablets, 210 mg , 200-count bottles, RX ONLY, Manufactured for and distribuDecember 12, 2017