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Health product recall

BD Phoenix™

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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