Artis zee Ceiling System (2018-10-03)

Starting date:

October 3, 2018

Posting date:

October 19, 2018

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-68046

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  Reason
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  Affected products

Affected products

Artis zee Ceiling System

Reason

During regular product monitoring abrasion was identified at the cabling at some Artis Zee Ceiling Systems. Abrasion may occur in the area of the cable outlet at the interior C-Arm. This is not a systematic issue but occurs sporadically at single units during the lifetime of a system. Siemens will be exchanging the existing cable routing at the C-Arm to prevent cable damage in future.

Affected products