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.
Take action
Contact the company
📍Recalling firmBaxter Healthcare Corporation1 Baxter Pkwy · Deerfield, IL 60015-4625
✎ GovInfoNow plain-language explainer
Baxter Healthcare is recalling Welch Allyn CP150 Electrocardiograph models with spirometry option because a critical EMI absorber was omitted during manufacturing. This could cause the device to malfunction or become vulnerable to electromagnetic interference, which might affect other medical devices or patient monitoring. Read more at govinfonow.com/recall/54932-welch-allyn-cp150-electrocardiograph-recall-emi-absorber-omission-risk.
“Welch Allyn CP150 Electrocardiograph Recall: EMI Absorber Omission Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54932-welch-allyn-cp150-electrocardiograph-recall-emi-absorber-omission-risk. Based on FDA recall #Z-2323-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2323-2024%22&limit=1).
Baxter Healthcare Corporation recalled one Welch Allyn CP150 Electrocardiograph with Spirometry Option on June 3, 2024, according to the FDA. The device may malfunction due to an omitted Electromagnetic Interference absorber installed during manufacturing.
How to tell if you have it
Brand: Welch Allyn
Product: CP150 Electrocardiograph with Spirometry Option
Product Code: CP150A-1ENB
Serial Number: 100013892024
UDI/DI: 00732094177640
The hazard
The omission of the Electromagnetic Interference (EMI) Absorber may allow EMI leakage that could affect other nearby devices or cause the unit itself to malfunction or become unavailable. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Baxter Healthcare Corporation has 187 other recalls on record since September 2, 2015. Other recent recalls of similar products include PRO+ MRS SURFACE FOR VERSACARE (August 18, 2026), 0.9% Sodium Chloride Injection (August 17, 2026), and Dextrose 2000mL Bags (August 17, 2026). Other recent recalls of similar products include Canon Vantage Galan 3T Medical Device (October 16, 2025), Philips Brilliance CT 64 Medical Scanner (August 7, 2026), and Boston Scientific LUX-DX II Arrythmia Detector (March 30, 2026).
How to tell if you have this one
Check for the product code CP150A-1ENB on the device. The device is sold as a single unit with spirometry option for cardiac monitoring. Serial numbers start with 100013892024.
Brand
Welch Allyn
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Details
Verify the product code (CP150A-1ENB) and serial number (starting with 100013892024) to confirm if your device is affected.
Where it went and when
Where it was distributed
Distributed in Illinois.
Listed by the agency
Not listed
FDA distribution: “Distribution to Illinois.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA published this recall 44 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2323-2024 (June 3, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2323-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.