HarmonyAIR Monitor Carrier (REF HCLP120004)Recalls & reported problems
Steris Corporation · The HarmonyAIR Monitor Carrier 4 Front Facing Mount, Low Profile, 1200mm Arm is a monitor mounting system designed for complex procedural environments. · Class 1
All models of HarmonyAIR (240)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00724995153380), received between Mar 2, 2023 and May 28, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (3 reports).
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
- Detachment of Device or Device Component3
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Laceration(s)1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 28, 2026Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE AN EMPLOYEE WAS MOVING THE MONITOR CARRIAGE TO THEIR HARMONYAIR MONITOR CARRIER INTO POSITION AND CONTACTED THE LOWER BOOM CAUSING THE MONITOR CARRIAGE COVER TO DETACH. A SHORT PROCEDURE DELAY WAS REPORTED. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25318981 ↗MalfunctionMay 21, 2026Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT AN EMPLOYEE WAS MOVING THE MONITOR CARRIAGE TO THEIR HARMONYAIR MONITOR CARRIER INTO POSITION AND CONTACTED THE LOWER BOOM CAUSING THE MONITOR CARRIAGE COVER TO DETACH AND CONTACT THE EMPLOYEE'S HEAD. NO MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED AND THE EMPLOYEE CONTINUED WORKING. NO INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25243226 ↗MalfunctionMar 2, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE END COVER TO THEIR HARMONYAIR MONITOR CARRIER DETACHED FROM THE SPRING ARM, MAKING CONTACT WITH THE SIDE OF AN EMPLOYEE'S FACE, RESULTING IN AN INJURY (LACERATION). MEDICAL TREATMENT WAS SOUGHT AND ADMINISTERED. NO REPORT OF PROCEDURE DELAY.
Patient problems: Laceration(s)
MAUDE report 16466731 ↗
Other TABLE, OPERATING-ROOM, AC-POWERED devices
- ORT300 TableIMRIS Imaging, Inc. · Table, Operating-Room, Ac-Powered2 recalls21 reports
- ORT200 TableIMRIS Imaging, Inc. · Table, Operating-Room, Ac-Powered2 recalls12 reports
- MEERA mobile operating table 720001F2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- MEERA mobile operating table 720001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall19 reports
- MAGNUS operating table system 118001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall17 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.
How reports and recalls are matched · Editorial policy · Report an error on this page