BD Vacutainer Tube Sodium Fluoride/Potassium Oxalate
Brand(s)
Last updated
Summary
Product
BD Vacutainer Tube Sodium Fluoride/Potassium Oxalate
Issue
Medical devices - Performance issue
What to do
Review recall notice, extend recall to any affected customers, return response forms.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
BD Vacutainer Tube Sodium Fluoride/Potassium Oxalate |
All lots. |
367001 |
Issue
The affected product ref 367001, BD vacutainer tube sodium fluoride: 100 mg, potassium oxalate: 20 mg, gray top, 10 ml contains isobutylene (also known as isobutene or 2-methylpropene) which in a recent publication demonstrated potential interference in determination of methanol by gas chromatography (GC) methods. Other non-GC methods are not impacted.
Recall start date: September 15, 2022
Additional information
Details
Original published date: 2022-09-28
Alert / recall type
Health product recall
Category
Health product - Medical device - General hospital and personal use
Companies
Becton Dickinson And Company
1 Becton Drive, Franklin Lakes, New Jersey, United States, 07417
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-64586