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Sunrise Medical MPD

FDA adverse event reports naming Sunrise Medical MPD as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SUNRISE MEDICAL MPD.

Total reports
2,335
Deaths
2
Injuries
9
Malfunctions
2,322

Reports per year

98
99
00
02
03

Source: FDA adverse event reports by year received, 19982003. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.

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Recent recalls

No recalls listed in the FDA device recall database for this entry.

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