Welch Allyn CP150 Electrocardiograph (Baxter) – EMI Absorber Missing (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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.
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
UDI/DI: 00732094177640. Product Code: CP150A-1ENB. Serial Number: 100013892024
Products Sold
UDI/DI: 00732094177640. Product Code: CP150A-1ENB. Serial Number: 100013892024
Baxter Healthcare Corporation is recalling Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150A-1ENB. The Electroc due to During manufacturing, the step to install an Electromagnetic Interference (EMI) Absorber was omitted. The purpose of the EMI absorber is to prevent EM. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
On 06/03/2024, Baxter Healthcare's Customer Service team contacted the consignee, via telephone call, to discuss the recall action and request the affected unit be returned to Baxter.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IL
Page updated: Jan 10, 2026