Class II — Steris Corporation
| Recalling firm | STERIS Corporation |
|---|---|
| Registered facility | Key Surgical, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach. |
| Product | ALYON Surgical Lighting System |
| Quantity | 549 units |
| Distribution | Worldwide - US Nationwide distribution. |
| Initiated | 2026-05-15 |
| Classified | 2026-06-15 |
| Recall number | Z-2450-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Steris Corporation (Z-2450-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98768/
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