Hill-rom Ritter
FDA adverse event reports naming Hill-rom Ritter as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: HILL-ROM RITTER.
- Total reports
- 20,057
- Deaths
- 45
- Injuries
- 104
- Malfunctions
- 19,468
Reports per year
15702
3503
5104
8705
7106
3407
4,72308
8,18009
6,71910
Source: FDA adverse event reports by year received, 2002–2010. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Bed, Ac-Powered Adjustable HospitalFNL16,010
- Stretcher, WheeledFPO2,140
- Table, Obstetrical, Ac-Powered (And Accessories)HDD1,803
- Table, Obstetric (And Accessories)KNC38
- Stretcher, Wheeled, PoweredINK32
- Bed, ManualFNJ14
- Product code ------3
- Bed, Pediatric Open HospitalFMS3
- Mattress, Air Flotation, Alternating PressureFNM3
- Chair And Table, MedicalKMN3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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