Vacuette 4 Ml Fx Sodium Fluoride / Potassium Oxalate Tube
Brand(s)
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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