Oakdale
FDA adverse event reports naming Oakdale as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: OAKDALE.
- Total reports
- 2,677
- Deaths
- 2
- Injuries
- 5
- Malfunctions
- 2,670
Reports per year
118
119
520
16421
1,39922
1,10723
Source: FDA adverse event reports by year received, 2018–2023. 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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