DELFIA Xpress (2018-11-01)

Starting date:

November 1, 2018

Posting date:

November 28, 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-68402

• 
  Reason
• 
  Affected products

Affected products

DELFIA Xpress

Reason

The bushing components of the sample tube racks, delivered with the instrument, are deficient; the plastic compound of the bushing component omitted a required ingredient. The deficiency causes tilting of the sample tubes.

Affected products