HexaPOD evo Module (2018-05-14)

Starting date:

May 14, 2018

Posting date:

May 25, 2018

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-66868

• 
  Reason
• 
  Affected products

Affected products

HexaPOD evo Module

Reason

After completion of a 6d workflow, the HexaPOD evo module may be in a tilted state if it is moved to the position used for 3d (non-iguide) treatments. During subsequent, non-image-guided 3d workflows, it is possible an incorrect position of the patient is difficult to detect.

Affected products