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ALYON

STERIS CORPORATION · Model ALYON Surgical Lighting System · UDI-DI 00724995225742

FSY
10
510(k) clearances
5,203
Adverse events
453
Recalls
67
Facilities

Description

The ALYON HD Single Light, Dual Accessory, Tandem is used with the ALYON Lighting System

Recalls

DateFirmReason
2026-05-15Steris CorporationThere is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.
2026-05-15Steris CorporationThe the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
2026-05-15Steris CorporationThe the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
2026-02-23Stryker CommunicationsSurgical light assembly may not adequate support the weight of the ceiling cover.
2025-07-15Stryker CommunicationsSurgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.
2025-06-23Steris CorporationThe DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detac
2025-06-23Steris CorporationThe DFPM yoke assembly ("yoke assembly") may detach from the spring arm. Should the yoke assembly detach from the spring arm, the yoke assembly would not be expected to fully detac
2024-07-09DKK Dai-Ichi Shomei Co., Ltd.The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.
2024-07-09DKK Dai-Ichi Shomei Co., Ltd.The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.
2024-07-09DKK Dai-Ichi Shomei Co., Ltd.The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.