EDS Light Suspensions, Central Axis (2018-11-21)

Starting date:

November 21, 2018

Posting date:

December 10, 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-68552

• 
  Reason
• 
  Affected products

Affected products

EDS Light Suspensions, Central Axis

Reason

Manufacturer had become aware that there was a remote likelihood that the EDS Light Suspensions, Central Axis may have an insufficiently assembled joint in the suspension.

Affected products