Welch Allyn CP150 Electrocardiograph with Spirometry Option — Class II medical device recall Z-2323-2024
Ongoing recall by Baxter Healthcare Corporation, reported 2024-07-17, distributed in IL. During manufacturing, the step to install an Electromagnetic Interference (EMI) Absorber was omitted. The purp
| Recall number | Z-2323-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2024-06-03 |
| Classified | 2024-07-10 |
| Reported by FDA | 2024-07-17 |
| Distributed | IL |
| Quantity | 1 units |
| Reason classes | packaging, device malfunction |
| UPC / GTIN / UDI-DI | 00732094177640 |
| Serial numbers | 100013892024 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2323-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.