- Recalling firm
- Steris Corporation
- Reason for recall
- The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
- Affected products (lot / model / serial)
- 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
- Units affected
- 549 units
- Distribution pattern
- Worldwide - US Nationwide distribution.
- Firm location
- Mentor, OH, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2450-2026
- Recall initiated
- May 15, 2026
- FDA classification date
- June 15, 2026
- FDA report date
- June 24, 2026
- FDA event ID
- 98768
- Last updated on HTM Vibe
- July 23, 2026