# FDA recall Z-2323-2024

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2024-06-03.

## Product

Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150A-1ENB. The Electrocardiograph is one of the tools that clinicians use to evaluate, diagnose, and monitor patient cardiac function.

## Reason for recall

During manufacturing, the step to install an Electromagnetic Interference (EMI) Absorber was omitted. The purpose of the EMI absorber is to prevent EMI leakage that might potentially affect other devices in the vicinity or the device itself may be vulnerable to EMI resulting in device malfunction or unavailability.

## Distribution

Distribution to Illinois.

## Key facts

- **Recall number:** Z-2323-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-03
- **Report date:** 2024-07-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2323-2024

## Citation

> AI Analytics. FDA recall Z-2323-2024. Retrieved 2026-07-28 from https://api.ai-analytics.org/recall/Z-2323-2024. Source: US FDA. Licensed CC0.

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