Class II

Medical Device Recall: HarmonyAIR A-Series Surgical Lighting System

Steris Corporation · May 15, 2026

Reason for Recall

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

Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Canada, India, New Zealand, Panama.

States Affected

NATIONWIDE

Quantity Affected

4138 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2448-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.