FDA Device recall Z-0072-2021
Change Healthcare Radiology Solutions 14.0
- FDA Device
- Class II
- terminated
- Published 2020-10-14
On 2020-10-14 the FDA classified a Class II recall of Change Healthcare Radiology Solutions 14.0 by Change Healthcare Canada, citing software defect which may potentially result in one or more images missing in a study.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0072-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-08-25 |
| Published | 2020-10-14 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Change Healthcare Canada |
| Distribution | MS, NE, VT, WV |
Product
Change Healthcare Radiology Solutions 14.0
Reason
Software defect which may potentially result in one or more images missing in a study
Identifiers
| code_info | All Model number 14.0 UDI (01)17540262030020(10)140000 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Other recalls by Change Healthcare Canada
- Change Healthcare Radiology Solutions software version 14.2.2
FDA Device · Class II · 2025-10-08 · Change Healthcare Canada - Change Healthcare Cardiology Hemodynamics Software
FDA Device · Class II · 2025-07-09 · Change Healthcare Canada - Change Healthcare Cardiology Hemo Software
FDA Device · Class II · 2025-07-09 · Change Healthcare Canada - Change Healthcare Cardiology Hemo
FDA Device · Class II · 2024-10-23 · Change Healthcare Canada - McKesson Cardiology Hemo
FDA Device · Class II · 2024-10-23 · Change Healthcare Canada
All Change Healthcare Canada recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0072-2021%22
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