Baxter Healthcare Corporation: Medical Device Recall in 2024 - (Recall #: Z-2323-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.
Product Description:

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.

Product Classification:

Class II

Date Initiated: June 3, 2024
Date Posted: July 17, 2024
Recall Number: Z-2323-2024
Event ID: 94805
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.

Status: Ongoing
Product Quantity: 1 unit
Code Information:

UDI/DI: 00732094177640. Product Code: CP150A-1ENB. Serial Number: 100013892024

Distribution Pattern:

Distribution to Illinois.

Voluntary or Mandated:

Voluntary: Firm initiated