Two-Lumen Central Venous Catheterization Set (2019-01-09)

Starting date:

January 9, 2019

Posting date:

January 25, 2019

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-68932

• 
  Reason
• 
  Affected products

Affected Products

Two-Lumen Central Venous Catheterization Set

Reason

The product Lidstock contains a labelling error. The Lidstock states the incorrect priming volume. The priming volumes printed on the extension lines are correct.

Affected products