BD Phoenix™
Brand(s)
Last updated
Summary
Product
BD Phoenix™
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
BD Phoenix™ 100 |
More than 10 numbers, contact manufacturer. |
448100 |
BD Phoenix™ M50 Instrument |
More than 10 numbers, contact manufacturer. |
443624 |
Issue
BD identified through post-market surveillance an increase in the number of complaints for Escherichia coli (E. coli) misidentification for clinical samples that were tested on BD Phoenix™ M50 instrument and BD Phoenix™ 100.
Recall Start Date: August 1, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Microbiology
Health products - Medical devices - Ophthalmology
Companies
Becton Dickinson And Company (BD)
7 Loveton Circle, Sparks, Maryland, United States, 21152
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75932
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