MAGNETOM Sola (2020-02-27)

Starting date:

February 27, 2020

Posting date:

March 13, 2020

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-72581

Last updated: 2020-03-19

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  Reason
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  Affected products

Affected Products

MAGNETOM Sola

Reason

The software update to NX VA20A resolves the following issues and prevents them from recurring. The update is not providing new features or new functionality. These fixes do not affect patient safety.

• Several improvements for PACS export
• Various Dicom tag and image text corrections
• Table position using select & go autopositioning corrected
• Image quality using save-as-series improved
• Prior study handling improved
• Orientation of composed spine images corrected
• General stability & performance improvements in:
• Patient registration
• Workflow configuration and execution
• System boot and shutdown

Affected products