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Health product recall

Vacuette * K2 EDTA

Last updated

Summary

Product
Vacuette * K2 EDTA
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Vacuette * K2 EDTA

B2205347
B220634A

454209

Issue

Some lot numbers of collection tubes Vacuette * K2 EDTA have experienced an issue of clotting. This was caused by insufficient amounts of EDTA additive sprayed in the tubes.

Recall start date: March 7, 2023

Additional information

Details
Original published date: 2023-03-23
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Greiner Bio One North America, Inc.

4238 Capital Drive, Monroe, North Carolina, United States, 28110

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-73376