Baxter Healthcare Corporation 2024-11-13 Health serious FDA
Health · FDA · Recall #FDA-Z-0323-2025
Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph Recall
Issued November 13, 2024 · Baxter Healthcare Corporation
In November 2024, Baxter Healthcare Corporation recalled the Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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 you should do
- 1 Stop using Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Baxter Healthcare Corporation to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Baxter Healthcare Corporation
- Category
- Health
- Recall date
- November 13, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution.
- Recall number
- FDA-Z-0323-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Baxter Healthcare Corporation has 36 recalls in our database, including 5 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.