Health product recall

Vacuette * K2 EDTA

Dernière mise à jour

Summary

Produit
Vacuette * K2 EDTA
Problème
Medical devices - Performance issue
Ce qu’il faut faire

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

Problème

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
Type d’avis ou de rappel
Health product recall
Catégorie
Health product - Medical device - General hospital and personal use
Entreprises

Greiner Bio One North America, Inc.

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

Published by
Health Canada
Audience
Healthcare
Classe de rappel
Type II
Identification number
RA-73376