# FDA recall Z-0733-2023

> **GE Medical Systems, LLC** · Class II · device recall initiated 2022-11-16.

## Product

B125M Patient Monitor, REF 6160000-005-XXXXXXX

## Reason for recall

GE Healthcare has become aware that if certain B1x5P / B1x5M patient monitors use "mmHg" or "kPa" as the unit for CO2 measurement, the displayed value for CO2 measurement can be inaccurate when used in a location that is not at or near sea level.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-0733-2023
- **Recalling firm:** GE Medical Systems, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-11-16
- **Report date:** 2022-12-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukesha, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0733-2023

## Citation

> AI Analytics. FDA recall Z-0733-2023. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0733-2023. Source: US FDA. Licensed CC0.

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