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
- 1,387
- Deaths
- 0
- Injuries
- 36
- Malfunctions
- 1,351
Reports per year
316
1017
1918
2719
3720
2021
1722
72624
40225
12626
Source: FDA adverse event reports by year received, 2016–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, Air, Non-Manual, For EndoscopeFEQ1,143
- Accessories, Photographic, For Endoscope (Exclude Light Sources)FEM180
- Apparatus, Suction, Ward Use, Portable, Ac-PoweredJCX33
- Endoscopic Access Overtube, Gastroenterology-UrologyFED12
- Cleaner, Ultrasonic, Medical InstrumentFLG8
- Endoscopic Bite BlockMNK8
- Endoscopic Irrigation/Suction SystemOCX2
- Cabinet, Table And Tray, AnesthesiaBRY1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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