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ProciseDx Calibration Cartridge

Chembio Diagnostic Systems Inc. · Model 5429 · UDI-DI 08100322954295

DCK
10
510(k) clearances
7
Adverse events
17
Recalls
45
Facilities

Description

The ProciseDx Calibration Cartridge is an accessory with quantitative assigned values to the ProciseDx Analyzer and is used to confirm that the instrument is operating within specified limits. The calibration cartridge does not contact biological specimens and is not used for diagnostic testing. The intended users are clinical laboratory professionals responsible for completing a periodic calibration check of the ProciseDx Analyzer.

Recalls

DateFirmReason
2025-04-14Ortho-Clinical Diagnostics, Inc.Product was incorrectly assigned GEN 88 instead of GEN 83 on product carton, foil wrapper, and cartridge (cart) label.
2024-10-11Ortho-Clinical Diagnostics, Inc.May Generate Negatively Biased Results When Testing Samples with High Concentrations of CRP, showing less than upper AMI of 90 mg/L (in the 70-90 mg/L range) while the samples havi
2023-02-01Randox LaboratoriesThe Antibody (R2 reagent) is showing a positive bias compared to previous batches on patient samples. Quality Controls do not show the same bias and will be within range
2016-10-26Ortho-Clinical DiagnosticsCRP samples diluted using VITROS Chemistry Products Specialty Diluent, VITROS Chemistry Products FS Diluent Pack 3, or a sample with a low concentration of CRP had positively biase
2013-06-12Ortho-Clinical DiagnosticsOrtho Clinical Diagnostics is recalling Slide Dispense cartridges used with some VITROS Chemistry Product Slides due to slide dispense issues.
2013-05-09Ortho-Clinical DiagnosticsWhile performing interval testing Ortho Clinical Diagnostics (OCD) determined that an excess amount of surfactant was unintentionally added to VITROS Chemistry Products CRP Slides
2013-03-06Alere San Diego, Inc.The Alere Cholestech LDX hsCRP cassette (PN 12-807) may have increased imprecision relative to the performance data in the package insert, which may cause differences in quantitati
2009-07-21Medtest Holdings, Inc.Individual vials of calibrator and standard were mislabeled; specifically the units on the vial labels are incorrectly listed as mg/dl when the correct unit is mg/L.
2009-05-01Kamiya Biomedical Company, LLCThe long-term stability of level 2 (1.0 mg/dL) may not be within the specifications due to a decrease in CRP concentration.
2008-01-10Beckman Coulter IncIMMAGE CRP Reagent lots M705441, M709279, & M709319, may demonstrate a prozone or hook effect on samples with extremely high CRP analyte concentration.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.