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HarmonyAIR G-Series SuspensionRecalls & reported problems

Steris Corporation · The G5 Dual Light with Dual Single Flat Panel Monitor, High Density Camera Ready is used with the HarmonyAIR G-Series Lighting System. · Class 2

All models of HarmonyAIR (240)

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 00724995192457), received between Dec 15, 2022 and Dec 15, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Flaked” (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

  • Flaked1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 15, 2022Flaked; Flaked

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE A PAINT CHIP FROM THEIR HARMONYAIR G-SERIES SURGICAL LIGHTING SYSTEM FELL INTO THE STERILE FIELD. USER FACILITY PERSONNEL REESTABLISHED THE STERILE FIELD SUBSEQUENTLY CAUSING A PROCEDURE DELAY; THE PATIENT PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15988373 ↗

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Sources and updates

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