Keymed (medical AND Industrial Equipment) Ltd.
FDA adverse event reports naming Keymed (medical AND Industrial Equipment) Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: KEYMED (MEDICAL AND INDUSTRIAL EQUIPMENT) LTD..
- Total reports
- 1,406
- Deaths
- 0
- Injuries
- 36
- Malfunctions
- 1,370
Reports per year
316
1017
1918
2719
3720
2021
1722
72624
40225
14526
Source: FDA adverse event reports by year received, 2016–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Pump, Air, Non-Manual, For EndoscopeFEQ1,159
- Accessories, Photographic, For Endoscope (Exclude Light Sources)FEM181
- Apparatus, Suction, Ward Use, Portable, Ac-PoweredJCX33
- Endoscopic Access Overtube, Gastroenterology-UrologyFED12
- Cleaner, Ultrasonic, Medical InstrumentFLG8
- Endoscopic Bite BlockMNK8
- Endoscopic Irrigation/Suction SystemOCX4
- Cabinet, Table And Tray, AnesthesiaBRY1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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