Vacuette * K2 EDTA
Brand(s)
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 |
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