Assay, Erythropoietin
Hematology · 21 CFR 864.7250
Recent MDR events
3 adverse event reports on file
Event type breakdown
Most-reported manufacturers
Recalls
5 recall events for this product code
- Beckman Coulter, Inc.Open, ClassifiedFeb 28, 2025
Access Erythropoietin (EPO), Catalog Number - A16364
Affected lot (439363) exhibited a negative dose drop of -22% with native patient samples compared to alternate reagent lots. Patient samples tested with the affected lot may demonstrate repeatable falsely decreased results, which may lead to improper diagnosis or repeat testing.
Z-1249-2025 · View FDA record ↗ - Siemens Healthcare Diagnostics, Inc.Open, ClassifiedMar 11, 2024
Atellica IM Erythropoietin (EPO) Assay (100 Test)
Siemens Healthcare Diagnostics has confirmed an average negative bias of -35% compared to the 3rd World Health Organization (WHO) International Standard (NIBSC code: 11/170) that is proportional across the assay measuring interval. The reference interval as claimed in the Instructions for Use (IFU) is not achieved with affected lots.
Z-1280-2024 · View FDA record ↗ - Siemens Healthcare Diagnostics, Inc.Open, ClassifiedMar 11, 2024
ADVIA Centaur Erythropoietin (EPO) Assay (100 Test)
Siemens Healthcare Diagnostics has confirmed an average negative bias of -35% compared to the 3rd World Health Organization (WHO) International Standard (NIBSC code: 11/170) that is proportional across the assay measuring interval. The reference interval as claimed in the Instructions for Use (IFU) is not achieved with affected lots.
Z-1281-2024 · View FDA record ↗ - R & D Systems, Inc.CompletedJul 15, 2022
Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations in human serum and pl
The Instructions for Use (IFU, Part Number 750095) provided with the affected lots by the firm contains an error associated with product s CE marking. The CE mark contained in the IFU is followed by the Notified Body designation, British Standards Institution number 2797 (BSI-2797) for product inserts 750095.28 and 750095.29. The erroneous label CE2797 were in the IFU insert revision 750095.28 for the 408 affected lots that were shipped. No product was packed with erroneous insert revision 750095.29. Since the product is currently CE marked as a Class I - self-certified product under the EU In Vitro Diagnostics Directive, the Notified Body designation should not be specified. As part of the corrective action, the firm has notified the customers who received the products with erroneous labeling, and is conducting the replacements with the correct product insert containing the Insert Revision 750095.30
Z-1390-2022 · View FDA record ↗ - Nichols Institute DiagnosticsTerminatedNov 15, 2005
Nichols Advantage EPO Calibration Verifiers, Catalog #63-7512
Some units in Lot 30-500953 (Calibration Verifier 2) are mislabeled as Calibration Verifier 3. Some units of Lot 30-500953 (Calibration Verifier 3) are mislabeled as Calibration Verifier 2.
Z-0136-06 · View FDA record ↗
Registered firms
12 firms currently registered for this product code
Beckman Coulter, Inc.
CHASKA, MN, US
Siemens Healthcare Diagnostics Inc.
Tarrytown, NY, US
Axis-shield Diagnostics, Ltd.
DUNDEE Scotland, GB
Biomerica
Irvine, CA, US
American Laboratory Products Company
Salem, NH, US
Drg International, Inc.
Springfield, NJ, US
Siemens Healthcare Diagnostics Products Limited
LLANBERIS Wales, GB
Drg Instruments Gmbh
MARBURG Hesse, DE
R & D Systems, Inc.
MINNEAPOLIS, MN, US
510(k) clearances
20 clearances for this product code
- Beckman Coulter, Inc.Apr 22, 2024
K240182 · Access EPO
- Axis-Shield Diagnostics LimitedAug 2, 2019
K183088 · ADVIA Centaur Erythropoietin (EPO) assay
- Beckman Coulter, Inc.Oct 6, 2006
K052223 · ACCESS EPO ASSAY
- Sangui Biotech, Inc.Jun 7, 2000
K992799 · SANGUI BIOTECH, INC. EPO (ERYTHROPOIETIN) ELISA KIT
- Diagnostic Products Corp.Jul 12, 1999
K983203 · IMMULITE EPO, MODEL #'S LKEPZ & LKEP1
- Nichols Institute DiagnosticsMar 23, 1999
K980737 · ADVANTAGE CHEMILUMINESCENCE ERYTHROPOIETIN IMMUNOASSAY
- Nichols InstituteMay 29, 1996
K952559 · ERYTHROPOIETIN IMMUNOASSAY KIT
- Genzyme Corp.Feb 5, 1996
K954898 · PREDICTA ERYTHROPOIETIN KIT (MODIFICATION)