Roche Molecular Systems, Inc. - Branchburg
FDA adverse event reports naming Roche Molecular Systems, Inc. - Branchburg as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG.
- Total reports
- 6,421
- Deaths
- 1
- Injuries
- 13
- Malfunctions
- 6,407
Reports per year
50320
3,85821
1,07922
32623
14524
43525
7526
Source: FDA adverse event reports by year received, 2020–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Reagents, 2019-Novel Coronavirus Nucleic AcidQJR3,431
- Covid-19 Multi-Analyte Respiratory Panel Nucleic Acid DevicesQLT1,652
- Respiratory Virus Panel Nucleic Acid Assay SystemOCC672
- Nucleic-Acid Tests Used For Infectious Disease Screening Of Blood And Plasma DonationsQHO401
- Somatic Gene Mutation Detection SystemOWD123
- Test, Hiv DetectionMZF63
- Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C VirusMZP18
- Test, Equipment, Automated Bloodborne PathogenMZA13
- Lab-Based Hiv Nat Diagnostic And/Or Supplemental TestQST11
- Clinical Sample ConcentratorJJH6
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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