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Tina-quant Transferrin ver. 2

Roche Diagnostics GmbH · Model 08058733190 · UDI-DI 07613336121573

DDG Prescription
1
510(k) clearances
2
Adverse events
6
Recalls
31
Facilities

Recalls

DateFirmReason
2022-06-09Randox Laboratories Ltd.A customer reported a problem with the reagent and calibrator. Randox Laboratories carried out an investigation and confirmed the issue. The complaint is pertaining to atypical cal
2022-06-09Randox Laboratories Ltd.A customer reported a problem with the reagent and calibrator. Randox Laboratories carried out an investigation and confirmed the issue. The complaint is pertaining to atypical cal
2019-08-28Roche Diagnostics Operations, Inc.Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for Rheumatoid Factors Interference
2019-08-28Roche Diagnostics Operations, Inc.Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for Rheumatoid Factors Interference
2018-05-16Abbott Laboratories, IncAn update to the Reagents and Specimen Collection and Handling/Preparation for Analysis sections of the IFU was required due to different issues with the various products.
2008-06-11Roche Diagnostics Corp.Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader.

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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.