Ingenia Elition X and S (2018-12-06)

Starting date:

December 6, 2018

Posting date:

January 8, 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-68688

• 
  Reason
• 
  Affected products

Affected products

1. Ingenia Elition X
2. Ingenia Elition S

Reason

Philips has become aware of a potential hazardous situation with the VitalScreen 'Stop Table' software button on the affected products (the yellow button on the right bottom corner). During automatic tabletop movement, pressing and holding the 'Stop Table' button may lead to an unexpected restart of the table movement.

Affected products