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Teco Diagnostics Total Protein Reagent Set

TECO DIAGNOSTICS · Model T528-480 · UDI-DI 10673486002201

CEK Prescription
1
510(k) clearances
94
Adverse events
10
Recalls
43
Facilities

Description

Teco Diagnostics Total Protein Reagent Set is used for the quantitative determination of total protein concentration in human serum.

Recalls

DateFirmReason
2025-08-11Siemens Healthcare Diagnostics, Inc.Potential for falsely depressed patient, quality control (QC), and/or calibration results or delayed results.
2024-07-29Siemens Healthcare Diagnostics, Inc.The potential for biased quality control (QC) and patient results when using Atellica CH UCFP lot 130414 and ADVIA Chemistry UCFP lot 140 reagents.
2024-07-29Siemens Healthcare Diagnostics, Inc.The potential for biased quality control (QC) and patient results when using Atellica CH UCFP lot 130414 and ADVIA Chemistry UCFP lot 140 reagents.
2023-01-27Siemens Healthcare Diagnostics, Inc.Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP), Triglycerides (Trig), and Triglycerides_2 (Trig_2) Impacting Magnesium (Mg) Results
2021-09-20Siemens Healthcare Diagnostics, Inc.The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Hemoglobin A1c (A1c_E and A1c_EM) results. Falsely de
2021-09-20Siemens Healthcare Diagnostics, Inc.The firm has confirmed the potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Hemoglobin A1c (A1c_E and A1c_EM) results. Falsel
2020-12-15Ortho Clinical Diagnostics IncEltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS XT Chemistry Products ALB-TP Slides
2020-12-15Ortho Clinical Diagnostics IncEltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS XT Chemistry Products ALB-TP Slides
2013-06-12Ortho-Clinical DiagnosticsOrtho Clinical Diagnostics is recalling Slide Dispense cartridges used with some VITROS Chemistry Product Slides due to slide dispense issues.
2003-03-26Ortho-Clinical DiagnosticsSlides may exhibit random, elevated imprecision of results.

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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.