Datascope Mahwah
FDA adverse event reports naming Datascope Mahwah as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DATASCOPE MAHWAH.
- Total reports
- 3,666
- Deaths
- 103
- Injuries
- 54
- Malfunctions
- 3,509
Reports per year
815
1916
1,07917
2,17518
38519
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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