EasyStand Evolv LargeRecalls & reported problems
Altimate Medical Inc. · Class 2
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 10858921006017), received between Dec 22, 2020 and Dec 22, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Device Handling Problem” (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.
Most reported problems
Device problems
- Device Handling Problem1
Patient problems
- Multiple Fractures1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 22, 2020Device Handling Problem; Device Handling Problem
EVALUATION EASYSTAND EVOLV LARGE FOLLOWING INCIDENT ON (B)(6) 2020. SERIAL NUMBER: (B)(4). DIAGNOSIS: CP, EPILEPSY. THE CLIENT BROKE HER RIGHT LEG ON TWO PLACES. TECHNICALLY, THE STANDING TABLE HAS BEEN CHECKED AND ALL SETTINGS CAN BE PROPERLY FIXED. THERE IS NO TECHNICAL PROBLEM, OR WEAR AND TEAR TO BE DISCOVERED ON THE STANDING TABLE, WHICH WOULD PREVENT CERTAIN PARTS FROM BEING FIXED. EVERYTHING WORKS AS IT SHOULD. SPOKEN WITH THE MANAGER AND ONE OF THE EMPLOYEES WHO TOOK THE CLIENT OUT OF THE STANDING TABLE, BUT IT IS NOT POSSIBLE FOR ME TO FIND OUT WHAT EXACTLY HAPPENED. THE EMPLOYEE REPORTS THAT SHE PUT THE CLIENT IN THE STANDING TABLE IN FRONT OF THE MIRROR WITH LIGHTS. THEN WALKED AWAY FOR A WHILE, WHEN SHE CAME BACK THE WHOLE STANDING TABLE HAD TURNED A QUARTER TURN AND THE WORKTOP WAS "GONE". THE CLIENT WAS COMPLETELY UNDER THE SEAT. IN THE PANIC TO GET THE CLIENT OUT OF THE STANDING TABLE AS QUICKLY AS POSSIBLE, ALL SETTINGS WERE OF COURSE CHANGED AND IT WAS ALSO NOT CLEAR FROM THE STORY HOW, FOR EXAMPLE, KNEE SUPPORTS OR WORKTOP STOOD. SHE INDICATES THAT SHE HAS CHECKED EVERYTHING BUT, FOR EXAMPLE, THE KNEE SUPPORTS ARE SET TO A CERTAIN DEPTH AND SHE SAID SHE NEVER TOUC
Patient problems: Multiple Fractures
MAUDE report 11059396 ↗
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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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