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IMPAX PACS
- Starting date:
- January 25, 2017
- Posting date:
- January 27, 2017
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type III
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-61996
Reason
Unexpected behavior can occur when the user selects patient studies for display.
A relevant prior study can unexpectedly display instead of the study selected.
If a prior study must be retrieved (because "relevance" is selected and the prior study is not readily available locally) and the retrieval of the prior study completes before the selected study is available for display, then the prior study will display instead of the selected (current) study.
Affected products
IMPAX PACS
Lot or serial number
- Software version 6.5.5
- Software version 6.6.1
Model or catalog number
- 6.5
- 6.6
Companies
- Manufacturer
-
AGFA Healthcare N.V.
Septestraat 27
Mortsel
2640
BELGIUM