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Steris Corporation recalls HarmonyAIR A-Series Surgical Lighting System
Recalled June 24, 2026 · FDA recall Z-2448-2026 · Steris
Hazard
There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads. · FDA Class II
Units
4138 units
Sold at
Worldwide distribution - US Nationwide and the countries of Australia, Canada, India, New Zealand, Panama.
Description
There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.
Product
HarmonyAIR A-Series Surgical Lighting System
Manufacturer(s)
Steris Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →