Health product recall

Vacuette 4 Ml Fx Sodium Fluoride / Potassium Oxalate Tube

Last updated

Summary

Product
Vacuette 4 Ml Fx Sodium Fluoride / Potassium Oxalate Tube
Issue
Medical devices - Performance issue
What to do

Contact Greiner Bio-One North America, Inc. 4238 Capital Drive Monroe, NC 28110
Email: RECALLS.US@GBO.COM

Affected products

Affected products Lot or serial number Model or catalogue number
Vacuette 4 Ml Fx Sodium Fluoride / Potassium Oxalate Tube A221135N 454297

Issue

Some tubes have no additive and clot.

Recall start date: December 13, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices
Companies
Greiner Bio One Gmbh
Bad Haller Strasse 32, Kremsmuenster, Austria, 4550
Published by
Health Canada
Audience
General public
Industry
Recall class
Type II
Identification number
RA-74885

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