ProductGuru Recalls

Official recall record

Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150A-1ENB. The Electrocardiograph is one of the tools that clin

US FDA — Medical Devices · 2024-06-03 · United StatesClass II
Issuing authority
US FDA — Medical Devices
Alert date
2024-06-03
Country of alert
United States
Alert level
Class II
Alert type
recall
Barcode (EAN/GTIN)
00732094177640
Brand on record
Baxter Healthcare Corporation

What the authority reported

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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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Other recalls from this brand

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