Baxter Healthcare Corporation recalls Hillrom Welch Allyn Vision Express Holter Analysis System software versions V6.1.0 to V6.4.1 due to potential duplicate patient ID assignments in medical records, which could cause misidentification of patient data.
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.
Baxter Healthcare Corporation is recalling Hillrom Welch Allyn Vision Express Holter Analysis System software versions V6.1.0 through V6.4.1. This recall is due to a potential risk of duplicate Unique Identifiers (UIDs) being assigned to patient exams, which could lead to misidentification of patient data when the system sends exams to Picture Archiving and Communication Systems (PACS).
The system may assign duplicate Unique Identifiers (UIDs) to patient exams. If the Picture Archiving and Communication System (PACS) relies solely on the UID to accept exams, this could cause patient identification mismatches with their physiological data, potentially leading to incorrect medical records.
Healthcare facilities that purchased or use the Hillrom Welch Allyn Vision Express Holter Analysis System software versions V6.1.0 to V6.4.1 are affected. Medical staff using these systems may be at risk of patient data misidentification.
Check for software versions V6.1.0 to V6.4.1 on the Hillrom Welch Allyn Vision Express Holter Analysis System. Units with specific UDI/DI numbers and serial numbers listed in the recall notice are affected.
Verify the software version on your Hillrom Welch Allyn Vision Express Holter Analysis System. If it is V6.1.0 to V6.4.1, it is affected.
Reach out to Baxter Healthcare Corporation for guidance on next steps if your system is affected.
The system may assign duplicate Unique Identifiers (UIDs) to patient exams, which could cause patient identification mismatches with their physiological data when the system sends exams to Picture Archiving and Communication Systems (PACS).
Check if your Hillrom Welch Allyn Vision Express Holter Analysis System software version is V6.1.0 to V6.4.1. Affected units have specific UDI/DI numbers and serial numbers listed in the recall notice.
Contact Baxter Healthcare Corporation for guidance on next steps if your system is affected.
We’ve drafted a message you can send Hillrom Welch Allyn to request your refund or repair — edit it as you like.
Subject: Recall Z-0323-2025 — Hillrom Welch Allyn Hillrom Welch Allyn Hello, I own a Hillrom Welch Allyn that is covered by recall Z-0323-2025 from Hillrom Welch Allyn. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
