← FDA ENFORCEMENT
Z-2450-2026Class II

Steris Corporation

Recalling firm
Steris Corporation
Product type
Device
Status
Ongoing
Report date
2026-06-24
Distribution
Worldwide - US Nationwide distribution.
Firm state
OH
Product quantity
549 units
Initiated by
Voluntary: Firm initiated
Reason for recall

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

Product description

ALYON Surgical Lighting System

Code / lot info

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

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.