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Tina-quant Hemoglobin A1cDx Gen.3

Roche Diagnostics GmbH · Model 08056668190 · UDI-DI 07613336120927

PDJLCP Prescription
10
510(k) clearances
208
Adverse events
9
Recalls
32
Facilities

Recalls

DateFirmReason
2026-06-08Siemens Healthcare Diagnostics, Inc.The potential for intermittent well-to-well bias on the A1c_E assay on the Atellica CH and Atellica CI analyzer which could cause falsely depressed or falsely elevated HbA1c patien
2026-02-23Siemens Healthcare Diagnostics, Inc.A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on separate analyzers are not imp
2023-04-17Ortho-Clinical Diagnostics, Inc.Potential for both unexpected positive and negative HbA1c results, may result in misdiagnosis
2022-06-09Abbott LaboratoriesThere is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
2022-06-09Abbott LaboratoriesThere is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
2022-06-09Abbott LaboratoriesThere is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c results to be generated using the ARCHITECT and Alinity c Hemoglobin A1c assay.
2022-02-09Siemens Healthcare Diagnostics, Inc.Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent carryover impacting quality control (QC), patient samples, and calibrator results.
2020-03-23Abbott Diagnostics Technologies ASThe analyzer system may have an electrostatic discharge and sparking of the power supply provided with the analyzers resulting in the power supply becoming non-functional.
2016-10-04Roche Diagnostics Operations, Inc..Roche Diagnostics has confirmed elevated QC and patient sample recovery for individual Tina-quant Hemoglobin A1c Gen.2 and Tina-quant Hemoglobin A1cDx Gen.2 cassettes/bottles. Thi

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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.