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Health Canada Medical devices

BD Phoenix™

Issued August 16, 2024
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
Hazard description
Performance
Product
Product name
BD Phoenix™
Reference
ID
RA-75932