ARTIS pheno (2021-05-26)

Starting date:

May 26, 2021

Posting date:

June 17, 2021

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-75813

Last updated:
2021-06-17

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  Reason
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  Affected products

Affected Products 

ARTIS pheno

Reason

The C‐arm might leave its intended travel path by up to 22 cm (9"), in cases of a fault within the drivetrain of an axis and while performing a stepped peripheral imaging (PERISTEPPING/PERIVISION).

Affected products