Quidel Corporation DBA Ortho-clinical Diagnostics
FDA adverse event reports naming Quidel Corporation DBA Ortho-clinical Diagnostics as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: QUIDEL CORPORATION DBA ORTHO-CLINICAL DIAGNOSTICS.
- Total reports
- 1,228
- Deaths
- 0
- Injuries
- 19
- Malfunctions
- 1,209
Reports per year
53024
60325
9526
Source: FDA adverse event reports by year received, 2024–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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