Health product recall

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

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

 VACUETTE 2 ml K2 EDTA

Lot or serial number

B21033DA

B21053R8

Model or catalog number

B21033DA

B21053R8

Companies
Manufacturer

Greiner Bio One North America

Inc.

4238 Capital Drive

North Carolina

UNITED STATES