Official recall record
HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video integration, and env
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2026-09-23
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00724995245047
- Brand on record
- Steris Corporation
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-10-22.
Record last checked against the registry on 2026-10-22.
Other recalls from this brand
- 2026-08-31 · US FDA — Medical Devices
VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007 - 2026-08-31 · US FDA — Medical Devices
VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061 - 2026-08-31 · US FDA — Medical Devices
VERIFY Biological Steam Test Pack Model/Catalog Number: S3069
ProductGuru Recalls republishes official safety information with attribution. We are not
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