Single (specified) Analyte Controls (assayed And Unassayed)
Clinical Chemistry · 21 CFR 862.1660
Recent MDR events
672 adverse event reports on file
- CONTOUR® NEXTJul 22, 2026MalfunctionAscensia Diabetes Care Us Inc.1810909-2026-00037
- MEDLINEJul 15, 2026MalfunctionMedline Industries, Lp1417592-2026-05224
- CONTOUR® NEXTJun 1, 2026MalfunctionAscensia Diabetes Care Us Inc.1810909-2026-00027
- CONTOUR® NEXTJun 1, 2026MalfunctionAscensia Diabetes Care Us Inc.1810909-2026-00030
- ELECSYS ANTI-HCV IIMay 26, 2026MalfunctionRoche Diagnostics1823260-2026-02066
- ALLIANCEApr 23, 2026MalfunctionMedline Industries, Lp1417592-2026-00354
- CONTOUR® NEXTApr 10, 2026MalfunctionAscensia Diabetes Care Us Inc.1810909-2026-00014
- ATELLICA IMFeb 13, 2026MalfunctionSiemens Healthcare Diagnostics Inc.1219913-2026-00038
- CONTOUR® NEXTFeb 2, 2026MalfunctionAscensia Diabetes Care Us Inc.1810909-2026-00005
- HCG/QUALJan 8, 2026MalfunctionSekisui Diagnostics, Llc24002943
Event type breakdown
Recalls
42 recall events for this product code
- Mckesson Medical-Surgical Inc. Corporate OfficeOpen, ClassifiedMay 27, 2025
SEKISUI DIAGNOSTICS LLC SERUM HCG OSOMGENZME CONTROL SET.
transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
Z-1854-2025 · View FDA record ↗ - Mckesson Medical-Surgical Inc. Corporate OfficeOpen, ClassifiedMay 27, 2025
HEMOCUE INC GLUC AQUEOUS 1HI/LO HEMCUE CONTROL KIT.
transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
Z-1855-2025 · View FDA record ↗ - Ortho-Clinical Diagnostics, Inc.Open, ClassifiedJun 4, 2024
VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro diagnostic use ly. For use in verifying the calibration range of the VITROS ECi/ECiQ/3600
The results generated by the VITROS Immunodiagnostic Products Vitamin B12 Range Verifier Lot# 1200 RV Level 2 may cause range verification failure. The issue is detectable by the user when the product fails to meet the required range during processing of RV Level 2 of this lot. There is a potential for a delay in patient test results should the user have a need to switch to an alternate method of range verification including use of an alternate lot. As this issue affects the upper limit range verification, there is no impact to VITROS Immunodiagnostic Products Vitamin B12 assay performance. Were the assay to not perform as expected, the failure would be detectable by Quality Control. Past patient sample results are unaffected, and no review of reported results is required.
Z-2019-2024 · View FDA record ↗ - Mckesson Medical-Surgical Inc. Corporate OfficeOpen, ClassifiedMar 19, 2024
Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set McKesson Consult" Pregnancy (hCG) Testing Positive Level / Negative Level 2 X 4 mL
Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 - 46.4 Degrees Fahrenheit (2 - 8 Degrees Celsius) for up to 60 minutes which could increase the probability of an incorrect test result or a delayed test result.
Z-1312-2024 · View FDA record ↗ - Ortho-Clinical Diagnostics, Inc.Open, ClassifiedJul 21, 2023
VITROS Immunodiagnostic Products NT-proBNP II Range Verifiers-For in vitro diagnostic use only. For use in verifying the calibration range of the VITROS ECi/ECi
May not meet the stability specifications for shelf life outlined in the Instructions For Use (IFU).
Z-2225-2023 · View FDA record ↗ - Siemens Healthcare Diagnostics, Inc.Open, ClassifiedFeb 21, 2023
ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells.
Negative bias occurred when whole blood calibration (Atellica IM Fol or ADVIA Centaur FolateBA/FolBA) used to test serum samples.
Z-1152-2023 · View FDA record ↗ - Siemens Healthcare Diagnostics, Inc.Open, ClassifiedFeb 21, 2023
ADVIA Centaur Folate 500 test kit- For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells.
Negative bias occurred when whole blood calibration (Atellica IM Fol or ADVIA Centaur FolateBA/FolBA) used to test serum samples.
Z-1153-2023 · View FDA record ↗ - Siemens Healthcare Diagnostics, Inc.Open, ClassifiedFeb 21, 2023
ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells.
Negative bias occurred when whole blood calibration (Atellica IM Fol or ADVIA Centaur FolateBA/FolBA) used to test serum samples.
Z-1154-2023 · View FDA record ↗ - Tosoh Bioscience IncTerminatedSep 14, 2020
Tosoh Bioscience AIA-PACK BHCG Calibration Verification Test Set-In Vitro Diagnostic for BHCG-pregnancy
Decreased stability for five (5) lots of Calibrator Sets and Calibration Verification Test Sets, resulting in a decrease measured concentration of HCG up to 20%.
Z-2968-2020 · View FDA record ↗ - Biochemical Diagnostics IncTerminatedNov 23, 2015
CONSULT(TM) diagnostics hCG CONTROLS Kit, Part/Reorder Number 5011, IVD
CONSULT diagnostics hCG Controls have discrepant storage temperatures listed on the kit labels when compared with the individual vial labels and the package insert.
Z-0328-2016 · View FDA record ↗
Registered firms
1,120 firms currently registered for this product code
Ortho Clinical Diagnostics, K.k.
Harumi, Chuo-ku Tokyo, JP
Abbott Gmbh
Wiesbaden Hesse, DE
Euroimmun Us Inc.
Mountain Lakes, NJ, US
Biokit S.a.
LLISSA D AMUNT Barcelona, ES
Lgc Clinical Diagnostics, Inc.
Cumberland Foreside, ME, US
Nova Biomedical Corporation Diabetes Products
Billerica, MA, US
Abbott Laboratories
Lake Forest, IL, US
Mka Medikal Ic Ve Dis Ticaret Sanayi Limited Sirketi
Cankaya Ankara, TR
Infrared Laboratory Systems Dba Synermed
WESTFIELD, IN, US
Ortho Clinical Diagnostics
Singapore South West, SG
Diazyme Laboratories, Inc.
POWAY, CA, US
Abbott Ireland Diagnostics Division
Longford, IE
Prevounce Health, Inc
Indianapolis, IN, US
Ascensia Diabetes Care Holdings Ag
Basel Basel-Stadt, CH
Roche Diagnostics Gmbh
MANNHEIM Baden-Wurttemberg, DE
Tosoh Aia, Inc.
TOYAMA, JP
510(k) clearances
493 clearances for this product code
- Roche DiagnosticsApr 4, 2017
K170678 · Beta-CrossLaps CalCheck 5
- Roche DiagnosticsJan 12, 2017
K162173 · Elecsys CYFRA 21-1 CalCheck 5
- Technopath ManufacturingOct 26, 2016
K162514 · Multichem A1c
- Aalto Scientific, Ltd.Aug 10, 2016
K161874 · Audit MicroControls Linearity DROP LQ Blood Glucose
- DiaSorin, Inc.Jun 30, 2016
K161522 · LIAISON EBV IgM Serum Control Set
- DiaSorin, Inc.Jun 30, 2016
K161526 · LIAISON CMV IgM Serum Control Set
- Immunodiagnostic Systems , Ltd.May 17, 2016
K161082 · IDS-iSYS 17-OH Progesterone Control Set, IDS-iSYS 17-OH Progesterone Calibration Verifiers
- Quantimetrix CorporationApr 21, 2016
K152117 · Dropper hsCRP High Sensitivity CRP Control