Steris Corporation recalls ALYON Surgical Lighting System
- Recalling company
- Steris Corporation
- Product
- ALYON Surgical Lighting System
- Reason
- The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- May 15, 2026
- Reported
- Jun 24, 2026
- Distribution
- Worldwide - US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 549 units
- Lot / codes
- 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
- Company location
- Mentor, OH
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2450-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2450-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.