MAGNETOM Terra (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-72579

Last updated: 2020-06-03

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  Reason
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  Affected products

Affected Products

MAGNETOM Terra

Reason

The software update to N4 VE12U-SH02 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.

• patient ID and name were not anonymized in error case.
• the pali shutdown test now considers factory tolerance of tales.
• PTX performance has been improved.

Affected products