EZ Smart Stand S400PS1-05Recalls & reported problems
EZ Way, Inc. · 400 lb. Smart Stand® with scale · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00848914007971), received between Jan 12, 2026 and Jan 12, 2026 — classified as 1 injury.
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
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Fall1
- Laceration(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 12, 2026Appropriate Device Problem Term/Code Not Available
CNA HAD HOOKED UP RESIDENT TO STAND USING LARGE HARNESS. LEFT HER HOOKED UP WHILE USING TOILET. WHEN DONE, RESIDENT CALLED FOR ASSISTANCE. SHE WAS RAISED TO ALMOST STANDING POSITION. DID PERICARE AND RESIDENT WAS STANDING FOR APPROXIMATELY 1 MINUTE BEFORE PULLING UP PANTS. CNA PULLED STAND AWAY FROM THE TOILET AND THE LEFT SIDE HARNESS LOOP CAME OFF. RESIDENT FELL BACKWARD AND HIT HEAD.
Patient problems: Fall; Laceration(s)
MAUDE report 24032058 ↗
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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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