Hill-rom Pluvigner
FDA adverse event reports naming Hill-rom Pluvigner as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: HILL-ROM PLUVIGNER.
- Total reports
- 2,438
- Deaths
- 1
- Injuries
- 4
- Malfunctions
- 2,423
Reports per year
205
106
307
6508
26909
31710
31211
43212
35513
47414
20815
Source: FDA adverse event reports by year received, 2005–2015. 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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