Steris Corporation - Montgomery
FDA adverse event reports naming Steris Corporation - Montgomery as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STERIS CORPORATION - MONTGOMERY.
- Total reports
- 1,587
- Deaths
- 2
- Injuries
- 23
- Malfunctions
- 807
Reports per year
9010
6411
10112
14013
14814
13015
9516
8617
10718
10519
6720
9121
9522
15623
4824
Source: FDA adverse event reports by year received, 2010–2024. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Table, Operating-Room, Ac-PoweredFQO855
- Light, Surgical, Ceiling MountedFSY258
- Table, Operating-Room, ElectricalGDC135
- Light, Surgical, AccessoriesFTA98
- Lamp, SurgicalFTD69
- Table, Surgical With Orthopedic Accessories, Ac-PoweredJEA28
- Light, Surgical, FiberopticFST21
- Table, Surgical With Orthopedic Accessories, ManualJEB18
- Warmer, Thermal, Infusion FluidLGZ18
- Table, Operating-Room, PneumaticFWW17
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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