SARA COMBILIZER APA1000-USRecalls & reported problems
Arjohuntleigh AB · SARA COMBILIZER - Early mobilisation moveable chair/table - powered · Class 1
Data updated Oct 18, 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 05055982788571), received between Mar 20, 2019 and Mar 20, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Electrical /Electronic Property 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 18, 2026.
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 20, 2019Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
ON 22 FEB 2019 ARJO WAS INFORMED ABOUT THE EVENT, WHICH OCCURRED IN (B)(6) HOSPITAL IN THE US. IT WAS REPORTED THAT DURING USING ARJO DEVICE- SARA COMBILIZER, THE EMERGENCY LOWERING FUNCTION DID NOT WORK WHEN THE PATIENT EXPERIENCED SHORTNESS OF BREATH AND THE RESUSCITATION WAS NEEDED. THE RESUSCITATION WAS PERFORMED IN THE STANDING POSITION. AFTER THAT, THE PATIENT WAS REMOVED FROM THE DEVICE. THE PATIENT DID NOT SUSTAIN ANY INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8435275 ↗
Other Table, Powered devices
- Trademark Elevating Table E9012-LPivotal Health Solutions, Inc. · Table, Powered1 recall3 reports
- HA90VHill Laboratories CO. · Table, Powered1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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