Staxi ST010-XRecalls & reported problems
Staxi Corporation · Staxi Standard Chair Color: Diamond Black · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00850039103216), received between Feb 17, 2026 and Feb 17, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Neck Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 17, 2026Detachment of Device or Device Component
REPORT OF A FRONT CASTER FALLING OFF CHAIR WHILST PASSENGER BEING PUSHED UP A INCLINE, CAUSING THE PASSENGER TO FALL FROM THE CHAIR.
Patient problems: Neck Pain
MAUDE report 24367235 ↗
Other Chair, Adjustable, Mechanical devices
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- Aquatec Ocean -VIP Kit Series 1470000Invacare Corporation · CHAIR, ADJUSTABLE, MECHANICAL1 death3 reports
- Raz Raz-CATRaz Design Inc · Chair, Adjustable, Mechanical2 reports
- DRIVEMEDICAL ATC17-BKDrive Devilbiss Healthcare · CHAIR, ADJUSTABLE, MECHANICAL1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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