Reported Jun 24, 2026 · Ongoing
ALYON Surgical Lighting System
Steris Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Steris Corporation · 5960 Heisley Rd · Mentor, OH · 44060-1834
Is this the product you have?
- ALYON Surgical Lighting System
- Lot codes and dates
- UDIs
00724995223182 0072499522313700724995223151007249952231750072499522289500724995222994 0072499522301400724995223021007249952230830072499522310600724995222758 0072499522312000724995223113007249952228400072499522303800724995223076 0072499522298700724995223007007249952227030072499522272700724995223090 0072499522571100724995225681007249952256980072499522572800724995222826 00724995222802007249952228570072499522269700724995222956and 00724995223229
- UDIs
- Amount recalled
- 549 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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