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HomeSTANBIO LABORATORY, L.P. › Total & Direct Bilirubin LiquiColor®

Total & Direct Bilirubin LiquiColor®

STANBIO LABORATORY, L.P. · Model 0260-200 · UDI-DI 00657498000601

CIG Prescription
10
510(k) clearances
399
Adverse events
19
Recalls
48
Facilities

Description

For the Quantitative Colorimetric Determination of Total and Direct Bilirubin in Serum or Plasma.

Recalls

DateFirmReason
2024-07-30Siemens Healthcare Diagnostics, Inc.During manufacturing, the last three tests from the 160 test flex of lot 23206BA (wells 8 or 10) were processed on the Dimension Vista platform. There was an issue with the filling
2023-08-05Ortho-Clinical Diagnostics, INc.Samples containing high levels of ALKP (or an interfering substance) could deplete the available substrate in the reagent layer of a VITROS ALKP Slide and not post the substrate de
2020-07-13Ortho-Clinical DiagnosticsEtrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS BuBc Slides and VITROS XT TBIL-ALKP Slides
2020-07-13Ortho-Clinical DiagnosticsEtrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS BuBc Slides and VITROS XT TBIL-ALKP Slides
2020-02-13Siemens Healthcare Diagnostics, Inc.Bilirubin assays may exhibit a positive bias with patients on eltrombopag therapy
2020-02-13Siemens Healthcare Diagnostics, Inc.Bilirubin assays may exhibit a positive bias with patients on eltrombopag therapy
2019-09-11Roche Diagnostics Operations, Inc.Due to low Quality Control recovery and invalid Calibration.
2019-08-15Beckman Coulter IncIt has been determined that N-acetyl p benzoquinone imine (NAPQI), a metabolite of acetaminophen (paracetamol), may cause negative interference for assays if present in high quanti
2019-08-15Beckman Coulter IncIt has been determined that N-acetyl p benzoquinone imine (NAPQI), a metabolite of acetaminophen (paracetamol), may cause negative interference for assays if present in high quanti
2018-12-17Roche Diagnostics CorporationNew endogenous interference claims have been established for the following assays used on the cobas c 311 analyzer and the cobas c 501, 502, 701, 702, and Modular Analytics P/D mod

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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.