Vacuette * K2 EDTA
Brand(s)
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 |
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 product - Medical device - 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