IGUIDE SOFTWARE 2.X INCLUDING WORKSTATION (2019-07-16)

Starting date:

July 16, 2019

Posting date:

August 2, 2019

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-70577

Last updated: 2019-08-02

• 
  Reason
• 
  Affected products

Affected Products

IGUIDE SOFTWARE 2.X INCLUDING WORKSTATION

Reason

Sometimes, although the HexaPOD has reached the target position, the Constant Correlation Check (CCC) can be too sensitive and iGUIDE may incorrectly demand a verification scan.

Affected products