FDA Device recall Z-2450-2026
ALYON Surgical Lighting System
- FDA Device
- Class II
- ongoing
- Published 2026-06-24
On 2026-06-24 the FDA classified a Class II recall of ALYON Surgical Lighting System by Steris, citing the the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2450-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-05-15 |
| Published | 2026-06-24 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Steris |
| Distribution | US |
Product
ALYON Surgical Lighting System
Reason
The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
Identifiers
| code_info | UDIs: 00724995223182 00724995223137, 00724995223151, 00724995223175, 00724995222895, 00724995222994 00724995223014, 007…UDIs: 00724995223182 00724995223137, 00724995223151, 00724995223175, 00724995222895, 00724995222994 00724995223014, 00724995223021, 00724995223083, 00724995223106, 00724995222758 00724995223120, 00724995223113, 00724995222840, 00724995223038, 00724995223076 00724995222987, 00724995223007, 00724995222703, 00724995222727, 00724995223090 00724995225711, 00724995225681, 00724995225698, 00724995225728, 00724995222826 00724995222802, 00724995222857, 00724995222697, 00724995222956, and 00724995223229 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2450-2026%22
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