Steris Corporation: Light, Surgical, Ceiling Mounted
Recall Summary Steris Corporation is recalling ALYON Surgical Lighting Systems because the plus and minus buttons (+/-) that control light intensity on the light heads may detach. The recall affects units distributed nationwide across the United States. This is classified as a Class II recall.
- Recalling firm
- 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
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-05-15
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Worldwide - US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ba2eeb5e-68e1-4067-9dc6-ed196ee10eb7