Artis Pheno (2020-01-02)

Starting date:

January 2, 2020

Posting date:

January 20, 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-72133

Last updated: 2020-01-21

• 
  Reason
• 
  Affected products

Affected Products

Artis Pheno

Reason

The potential exists for system movement to be permanently blocked by an activation of the collision sensor integrated in the cover of the collimator even when no collision has occurred.

Affected products