VACUETTE 2 ml K2 EDTA (2021-09-17)

Starting date:

September 17, 2021

Posting date:

October 22, 2021

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-76695

Last updated: 2021-10-22

• Reason
• Affected products

Affected Products

VACUETTE 2 ml K2 EDTA

Reason

The blood collection tubes have experienced an issue of clotting caused by no or inconsistent amounts of EDTA sprayed in the tubes.

Affected products