ProductGuru Recalls

Official recall record

Hillrom Welch Allyn Q-Stress Cardiac Stress Testing System; cardiac stress test

US FDA — Medical Devices · 2024-10-11 · United StatesClass II
Issuing authority
US FDA — Medical Devices
Alert date
2024-10-11
Country of alert
United States
Alert level
Class II
Alert type
recall
Barcode (EAN/GTIN)
00732094263213
Brand on record
Baxter Healthcare Corporation

What the authority reported

There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.

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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