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FDA
Food and Drug Administration · Recall Z-2448-2026 · May 15, 2026

HarmonyAIR A-Series Surgical Lighting System

Steris Corporation

The hazard

There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

HarmonyAIR A-Series Surgical Lighting System

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model UDIs: 00724995186388Model 00724995186401Model 00724995188320Model 00724995188481Model 00724995188467Model 00724995188498Model 00724995189433Model 00724995186562Model 00724995188696Model 00724995188627Model 00724995188610Model 00724995186074Model 00724995186081Model 00724995186302Model 00724995186319Model 00724995188269Model 00724995186371Model 00724995188634Model 00724995186326Model 00724995186067Model 00724995186548Model 00724995186579Model 00724995188580Model 00724995187149Model 00724995187170UPC 00724995186388UPC 00724995186401UPC 00724995188320UPC 00724995188481UPC 00724995188467UPC 00724995188498UPC 00724995189433UPC 00724995186562UPC 00724995188696UPC 00724995188627UPC 00724995188610UPC 00724995186074UPC 00724995186081UPC 00724995186302UPC 00724995186319UPC 00724995188269UPC 00724995186371UPC 00724995188634UPC 00724995186326UPC 00724995186067UPC 00724995186548UPC 00724995186579UPC 00724995188580UPC 00724995187149UPC 00724995187170

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.