Roche Molecular Systems, Inc.
18 devices · 224 adverse event reports · 2 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- cobas® EGFR Mutation Test v2 2.0Somatic gene mutation detection system129 reports
- cobas Liat Analyzer 07341920190real time Nucleic acid amplification system1 recall4 reports
- cobas z 480 05200881001DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA1 recall0 reports
- 41 reports
- cobas® HIV-1 09040803190Test, HIV detection27 reports
- cobas® HBV 09040820190Hepatitis Viral B DNA Detection5 reports
- cobas® PCR Media Uni Swab Sample Kit 07958030190DNA PROBE, NUCLEIC ACID AMPLIFICATION, CHLAMYDIA3 reports
- cobas® HIV-1/HIV-2 Qualitative 09040528190Test, HIV detection3 reports
- COBAS® AmpliPrep/ COBAS® TaqMan® HIV- 1 Test, version 2.0Test, hiv detection2 reports
- cobas® Influenza A/B & RSV Nucleic acid test for use on the cobas® Liat® System 08160104190Influenza A And Influenza B Multiplex Nucleic Acid Assay2 reports
- COBAS® AmpliPrep / COBAS® TaqMan® HBV Test, v2.0Hepatitis Viral B DNA Detection1 report
- cobas PCR Media Dual Swab Sample Kit 07958021190DNA-REAGENTS, NEISSERIA1 report
- cobas Factor II and Factor V Test 07948352190TEST, FACTOR II G20210A MUTATIONS, GENOMIC DNA PCR1 report
- 1 report
- cobas® HCV 09040765190Assay, hybridization and/or nucleic acid amplification for detection of hepatitis c rna,hepatitis c virus1 report
- cobas HPV 09040544190KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS1 report
- COBAS® AmpliPrep Instrument 03051315001CLINICAL SAMPLE CONCENTRATOR1 report
- COBAS® TaqMan® 03121453001ANALYZER, CHEMISTRY, MICRO, FOR CLINICAL USE1 report