Product Wiki · Recalls · Health Canada — Medical Devices

BD Phoenix™ — recall 75932

Health Canada — Medical Devices · Canada · 2024-08-16 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
75932
Date of alert
2024-08-16
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Microbiology - Ophthalmology
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: 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
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/bd-phoenixtm

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