Stryker Medical-kalamazoo
FDA adverse event reports naming Stryker Medical-kalamazoo as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: STRYKER MEDICAL-KALAMAZOO.
- Total reports
- 29,166
- Deaths
- 105
- Injuries
- 1,137
- Malfunctions
- 27,924
Reports per year
12,89813
3,48214
64615
42416
59617
1,45518
1,21719
1,22820
1,62721
1,23722
1,37523
1,42824
1,23025
32326
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Bed, Ac-Powered Adjustable HospitalFNL12,204
- Stretcher, WheeledFPO10,736
- Stretcher, Wheeled, PoweredINK1,244
- Bed, Pediatric Open HospitalFMS1,011
- Stretcher, Hand-CarriedFPP927
- Table, Obstetrical, Ac-Powered (And Accessories)HDD572
- System, Thermal RegulatingDWJ445
- Mattress, Flotation Therapy, Non-PoweredIKY338
- Bed, Patient Rotation, PoweredIKZ289
- Stool, Operating-RoomFZM271
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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