Change Healthcare Radiology Solutions 14.2.2Recalls & reported problems

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

3 other recalls cover devices cleared under the same FDA submission (K140909); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

1. Aug 13, 2025Class IIOpen, Classified

   Due to software issue, radiology reports may not be fully displayed when viewing.

   Z-0030-2026 · Root cause: Software Design Change · Recall details · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K140909. One submission often covers many models, so check the product and lot details in each record.

• Z-0237-2024 · Oct 12, 2023 · Open, Classified
  Change Healthcare Radiology Solutions, software versions 14.0, 14.1, and 14.2 Medical image and information management software.
• Z-0072-2021 · Aug 25, 2020 · Terminated
  Change Healthcare Radiology Solutions 14.0
• Z-1396-2017 · Dec 2, 2016 · Terminated
  McKesson Radiology 12.2 - Picture Archive Communication System (PACS)