Cios Alpha (2019-04-10)

Starting date:

April 10, 2019

Posting date:

April 29, 2019

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-69742

Last updated: 2019-04-30

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  Reason
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  Affected products

Affected Products

Cios Alpha

Reason

Siemens is providing an optimised set of FD calibration data to prevent the possibility of black fringes appearing in seldom cases and special circumstances at the border of objects/patients to direct radiation images.

Affected products