FDA Device recall Z-0118-2027
HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video integration, and en…
- FDA Device
- Class II
- ongoing
- Published 2026-10-14
On 2026-10-14 the FDA classified a Class II recall of HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video integration, and en… by Steris, citing 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 docu….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0118-2027 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-09-23 |
| Published | 2026-10-14 |
| Last updated | 2026-10-21 05:30 UTC |
| Company | Steris |
| Distribution | US |
Product
HexaVue Focus Integration System, a single, all-in-one system that handles operating room video routing, surgical video integration, and environmental control, Software Version: 2.0.18
Reason
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.
Identifiers
| code_info | Lot Code: UDI: 00724995245047; Serial Numbers: RL25293001 RL25301003 RL25301004 RL26007031 RL26013044 RL26013045 RL260…Lot Code: UDI: 00724995245047; Serial Numbers: RL25293001 RL25301003 RL25301004 RL26007031 RL26013044 RL26013045 RL26028062 RL26040066 RL26054029 RL26062001 RL26063005 RL26063007 RL26063013 RL26063014 RL26063019 RL26063021 RL26063022 RL26063023 RL26069033 RL26069034 RL26072049 RL26072052 RL26072053 RL26072055 RL26072056 RL26072056 RL26077072 RL26077073 RL26077074 RL26083077 RL26084078 RL26084080 RL26084081 RL26085083 RL26085084 RL26085085 RL26085086 RL26085087 RL26085088 RL26085089 RL26089090 RL26089091 RL26089092 RL26089093 RL26089094 RL26089095 RL26089096 RL26089097 RL26098098 RL26104099 RL26105102 RL26133103 RL26133104 RL26138105 RL26139106 RL26140114 RL26187116 RL26243121 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-10-21 05:30 UTC. Current status: ongoing.
Other recalls by Steris
- RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020116
FDA Device · Class II · 2026-10-21 · Steris - RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020117
FDA Device · Class II · 2026-10-21 · Steris - RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020115
FDA Device · Class II · 2026-10-21 · Steris - VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB006
FDA Device · Class II · 2026-10-14 · Steris - VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060
FDA Device · Class II · 2026-10-14 · Steris
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0118-2027%22
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