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FDA device recallVulnerabilitiesPublished October 7, 2026
Steris Corporation: Light, Surgical, Accessories
Updated under an hour ago ()
A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on printed images could create a documentation discrepancy or incorrect association of clinical images with a patient record.
- Tags
- FDA recall, medical device, class 2, General, Plastic Surgery, Software design, Open, Classified
- Related exam domains
- CISSP 3: Security Architecture and Engineering; CISSP 8: Software Development Security; CISA 3: Information Systems Acquisition, Development and Implementation; CISA 5: Protection of Information Assets
- Source record id
- Z-0118-2027
- First seen by InfoSec Signals
- 10/9/2026
Source: openFDA device recalls, U.S. Food and Drug Administration about this source more from it
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