ARTIS Q and Zee Ceiling (2018-02-02)

Starting date:

February 2, 2018

Posting date:

February 16, 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-65984

• 
  Reason
• 
  Affected products

Affected products

1. ARTIS ZEE CEILING
2. ARTIS Q

Reason

This update provides a corrective action in regards to the ceiling base rotation brake for select ARTIS systems. Special screws will be used for the brake adjustment. This corrective action is to address the issue with a component (adjustment screw supplied with a thread lock): a batch of non-compliant components was delivered (thread lock was missing).

Affected products