HarmonyAIR A-Series Surgical Lighting System: recall status

⚠ Recalls found. HarmonyAIR A-Series Surgical Lighting System is named in 2 official recalls in our current data:

FDA Class II recall Z-2448-2026 — There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.
FDA Class II recall Z-2449-2026 — The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

Brand: Steris

Recalls naming this model

FDA Class II · Medical device · June 24, 2026

HarmonyAIR A-Series Surgical Lighting System recall — Steris Corporation

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

Company / brand: Steris recalls

Affected product: HarmonyAIR A-Series Surgical Lighting System recall status

Official ID Z-2448-2026 · Official record ↗

FDA Class II · Medical device · June 24, 2026

HarmonyAIR A-Series Surgical Lighting System recall — Steris Corporation

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

Company / brand: Steris recalls

Affected product: HarmonyAIR A-Series Surgical Lighting System recall status

Official ID Z-2449-2026 · Official record ↗

See all Steris recalls →

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.