Masimo - 40 Parker
FDA adverse event reports naming Masimo - 40 Parker as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MASIMO - 40 PARKER.
- Total reports
- 2,491
- Deaths
- 16
- Injuries
- 36
- Malfunctions
- 2,439
Reports per year
315
46116
1,10217
59518
33019
Source: FDA adverse event reports by year received, 2015–2019. 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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