FDAOctober 11, 2024device

Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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