SchureMed 800-0142Recalls & reported problems
Schuerch Corporation · E-Z Lift Beach Chair · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00810014601885), received between May 17, 2023 and Sep 13, 2023 — classified as 2 malfunctions.
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.
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Device Fell1
Patient problems
- Fall2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 13, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE A NON-STERIS E-Z LIFT BEACH CHAIR DETACHED FROM THEIR STERIS 4085 SURGICAL TABLE WHILE ADJUSTING THE HEIGHT SUBSEQUENTLY CAUSING THE PATIENT TO FALL OFF THE TABLE. NO REPORT OF INJURY. THE PROCEDURE WAS CANCELLED.
Patient problems: Fall
MAUDE report 17739127 ↗MalfunctionMay 17, 2023Device Fell; Device Fell
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR NON-STERIS E-Z LIFT BEACH CHAIR WHICH WAS ATTACHED TO A STERIS SURGICAL TABLE FELL BACKWARDS RESULTING IN A PROCEDURE DELAY AND INJURY TO THE PATIENT'S NECK. IT IS UNKNOW IF MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Fall
MAUDE report 16948196 ↗
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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