Keryx Biopharmaceuticals, Inc. recalls
Every recall we track for Keryx Biopharmaceuticals, Inc. — 2 in all, from 2017–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for Keryx Biopharmaceuticals, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 1 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Keryx Biopharmaceuticals, Inc. product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Keryx Biopharmaceuticals, Inc. recalls
2 shown- UnratedDrug
Keryx Biopharmaceuticals, Inc. recalls Auryxia (ferric citrate) tablets 210 mg, Rx Only, 200 tablets per bottle, Manufactured for and distributed by: Keryx
Keryx Biopharmaceuticals recalls Auryxia 210mg tablets due to FDA manufacturing process deviations. Affected lots were not made per approved standards. Consumers should contact Keryx for details.
KeryxJul 10, 2020 - Lower riskDrug
Keryx Biopharmaceuticals, Inc. recalls Auryxia (ferric citrate) tablets, 210 mg , 200-count bottles, RX ONLY, Manufactured for and distributed by: Keryx
Keryx recalls 210mg Auryxia tablets (200-count) due to silica gel desiccant potentially contacting tablets. RX-only medication for iron deficiency.
KeryxDec 12, 2017
Keryx Biopharmaceuticals, Inc. recall questions
How many recalls has Keryx Biopharmaceuticals, Inc. had?
2 recalls from Keryx Biopharmaceuticals, Inc. are on record with U.S. safety agencies, from 2017–2020.
What is the most recent Keryx Biopharmaceuticals, Inc. recall?
Keryx Biopharmaceuticals, Inc. recalls Auryxia (ferric citrate) tablets 210 mg, Rx Only, 200 tablets per bottle, Manufactured for and distributed by: Keryx, dated Jul 10, 2020. Every Keryx Biopharmaceuticals, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Keryx Biopharmaceuticals, Inc. product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Keryx Biopharmaceuticals, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.