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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall OraQuick HCV Visual Reference Panel Immunology and Microbiology Devices OraSure Technologies, Inc. 3 United States USFDA
Device Recall Roche Molecular Systems Immunology and Microbiology Devices Roche Molecular Systems, Inc. 3 United States USFDA
Device Recall Dako HER2 CISH pharmDx Kit Immunology and Microbiology Devices Dako North America Inc. 3 United States USFDA
Device Recall Roche cobas 6800/8800 system, Hepatitis Viral B DNA Detection Immunology and Microbiology Devices Roche Diagnostics Operations, Inc. 3 United States USFDA
Device Recall IMMULITE/IMMULITE 1000 PSA Immunology and Microbiology Devices Siemens Healthcare Diagnostics, Inc. 3 United States USFDA
Device Recall IMMULITE/IMMULITE 2000 PSA Assay Immunology and Microbiology Devices Siemens Healthcare Diagnostics, Inc. 3 United States USFDA
Device Recall IMMULITE/IMMULITE 1000, Third Generation PSA Immunology and Microbiology Devices Siemens Healthcare Diagnostics, Inc. 3 United States USFDA
Device Recall IMMULITE/IMMULITE 1000 Third Generation PSA Immunology and Microbiology Devices Siemens Healthcare Diagnostics, Inc. 3 United States USFDA
Device Recall Her2/Neu (cerbB2) (CB11) Immunology and Microbiology Devices Cell Marque Corporation 3 United States USFDA
Device Recall Her2/Neu (EP3) Immunology and Microbiology Devices Cell Marque Corporation 3 United States USFDA
Device Recall IMMULITE 2000/IMMULITE 2000 XPi Anti HBc Immunology and Microbiology Devices Siemens Healthcare Diagnostics, Inc. 3 United States USFDA
Device Recall ADVIA Centaur HBc IgM Immunology and Microbiology Devices Siemens Healthcare Diagnostics, Inc. 3 United States USFDA
Digene''s Hybrid Capture 2 HPV DNA Test, Catalog # 5101-1096 Immunology and Microbiology Devices Digene Corp 3 United States USFDA
Digene''s Hybrid Capture 2 HPV DNA Test, Catalog # 5196-1230, labeled for export only. Immunology and Microbiology Devices Digene Corp 3 United States USFDA
Hybrid Capture 2 High-Risk HPV DNA Test, Catalog # 5101-1296 Immunology and Microbiology Devices Digene Corp 3 United States USFDA
Hybrid Capture II CT-ID Test, Catalog #5135-1050IVT, (labeled for export only). Immunology and Microbiology Devices Digene Corp 3 United States USFDA
Device Recall Abbott AxSYM AFP Immunology and Microbiology Devices Abbott Laboratories HPD/ADD 3 United States USFDA
Device Recall Architect AntiHBs Reagent Immunology and Microbiology Devices Abbott Laboratories HPD/ADD/GPRD 3 United States USFDA
Amplicor [3] AV-HRP. (Avidin-HRP (Horseradish Peroxidase) BGG Conjugate.) || Kit: Amplicor HCV Detection Kit, v2.0 Immunology and Microbiology Devices Roche Molecular Systems Inc 3 United States USFDA
Amplicor [3] AV-HRP, Avidin-HRP (Horseradish Peroxidase) BGG Conjugate. || Kit: AmpliCap HCV MonitorTest, Export, RUO. Immunology and Microbiology Devices Roche Molecular Systems Inc 3 United States USFDA
Device Recall Architect AntiHBs Reagent Immunology and Microbiology Devices Abbott Laboratories HPD/ADD/GPRD 3 United States USFDA
ELx800 microtiter plate reader software program written for use with ORTHO HCV Version 3.0 ELISA Test System. Immunology and Microbiology Devices Diasorin Inc. 3 United States USFDA
Vitros Immunodiagnostic HBsAg CONFIRMATORY KIT * REF 680 1324. Firm on label: Ortho-Clinical Diagnostics, 62 The Broadway, Amersham, Bucks, UK. UPC *+H221680132412* . Each kit contains: 1 x kit of reagents, and protocol card for HBsAg Confirmatory Kit. According to the firm (but not on label), there are 60 neutralization reactions per confirmatory kit. Immunology and Microbiology Devices Ortho-Clinical Diagnostics 3 United States USFDA
COBAS AmpliPrep / COBAS TaqMan HCV Test, USIVD Immunology and Microbiology Devices Roche Molecular Systems, Inc. 3 United States USFDA
COBAS AmpliPrep / COBAS TaqMan HCV Test, CEIVD Immunology and Microbiology Devices Roche Molecular Systems, Inc. 3 United States USFDA