---
title: "Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Ca... — FDA record Z-1492-2025 | Is It on Recall"
description: "During some clinical cases, it has been observed that the SO2 value may periodically appear as dashes on the Touchscreen Display indicating unavailable data. In"
url: https://isitonrecall.com/recall/fda-device-z-1492-2025-terumo-cdi-oneview-monitoring-system-hematocrit-oxygen-saturation-probe-catalog-number-ref-cd1754/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754 — FDA record Z-1492-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 3, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754
- **Reason**: During some clinical cases, it has been observed that the SO2 value may periodically appear as dashes on the Touchscreen Display indicating unavailable data. In these cases, a yellow low-limit alarm will also be triggered to the user, due to the dashed-out value.
- **Classification**: Class II
- **Recalling firm**: Terumo Cardiovascular Systems Corporation
- **Quantity**: 37 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1492-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1492-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI/DI 00886799001882, Serial Number range: H0050095-H0050110, H0050112-H0050116, H0050118-H0050124, H0050126, H0050131-H0050134, H0050136, H0050140-H0050142 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: IL, TX, NY, MI, FL, NV, and Australia, New Zealand

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Florida](https://isitonrecall.com/state/florida/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Michigan](https://isitonrecall.com/state/michigan/)
- [Nevada](https://isitonrecall.com/state/nevada/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Apr 9, 2025
- **Recall initiation date**: Mar 3, 2025
- **Center classification date**: Mar 31, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1492-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Terumo Cardiovascular Systems Corporation records](https://isitonrecall.com/brand/terumo-cardiovascular-systems-corporation/)