Class II

Medical Device Recall: HarmonyAIR A-Series Surgical Lighting System

Steris Corporation · May 15, 2026

Reason for Recall

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

Distribution

Worldwide - US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

2101 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2449-2026

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.

Steris Corporation Medical Device Recall: HarmonyAIR A-Series Surgical Lighting System | SafeCheck