Citadel CX812A3K1AMAD0Recalls & reported problems
Arjohuntleigh AB · Medical Bed - CITADEL - USA - with Indigo powered drive. · Class 2
All models of Citadel (3)
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 05056097351742), received between Apr 12, 2024 and Apr 12, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device 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.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Fall1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 12, 2024Use of Device Problem; Use of Device Problem
FOLLOWING THE INFORMATION GATHERED, THE PATIENT FELL FROM THE CITADEL BED. THE CUSTOMER ALLEGED THAT THE CITADEL BED EXIT ALARM WAS SET, BUT DID NOT TURN ON WHEN THE EVENT OCCURRED. THE EXIT ALARM IS DESIGNED TO NOTIFY THE STAFF WHEN THE PATIENT¿S UNDESIRED MOVEMENT OCCURS. IT DOES NOT PROTECT THE PATIENT FROM INTENTIONAL OR UNINTENTIONAL EXIT FROM THE BED. THE ARJO SERVICE TECHNICIAN CHECKED THE EXIT ALARM AND NO ISSUE WAS FOUND. THE CIRCUMSTANCES OF THE EVENT REMAIN UNKNOWN AS THE EVENT WAS UNWITNESSED. THERE WAS NO INJURY REPORTED BY A CUSTOMER.
Patient problems: Fall
MAUDE report 19095439 ↗
Other BED, FLOTATION THERAPY, POWERED devices
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- pro+ P7924ARENT01Hill-Rom, Inc. · Bed, Flotation Therapy, Powered3 recalls1 death15 reports
- pro+ P3255A02Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls8 reports
- pro+ P7924A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls4 reports
- pro+ P3255A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls3 reports
- pro+ P7923A03Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls2 reports
- pro+ P7923A01Hill-Rom, Inc. · BED, FLOTATION THERAPY, POWERED3 recalls0 reports
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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