Pediatric Two-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter (2018-11-12)

Starting date:

November 12, 2018

Posting date:

December 10, 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-68536

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  Reason
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  Affected products

Affected products

Pediatric Two-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter

Reason

Arrow International has voluntarily issued an advisory notice for the Pediatric Two-Lumen Central Venous Catheterization Set with Blue Flextip Catheter as the product Lidstock contains a labelling error. The Lidstock states the incorrect priming volume and flow rates.

Affected products