Health product recall

BBL Sensi-Disc Antimicrobial Susceptibility Test Discs

Last updated

Summary

Product
BBL Sensi-Disc Antimicrobial Susceptibility Test Discs
Issue
Medical devices - Device compatibility
What to do

Contact the manufacturer if you require additional information. 

Affected products

Affected products Lot or serial number Model or catalog number
BBL Sensi-Disc Antimicrobial Susceptibility Test Discs More than 10 numbers, contact manufacturer. 203705 231250 231274 231541 231607 231644 231653 231682 230733 231544 231634 231703 232174 231606 231673 231706 231251 231264 231635 231640 231657 231674 231696 231705 231263 231344 231628 231629 231641 231645
BBL Sensi-Disc Antimicrobial Susceptibility Test Discs More than 10 numbers, contact manufacturer. 231658 231664 231692 231758 232175 230998 231633 231678 231691 231536 231539 231621 231632 231660 231672 231704 232219 232231

Issue

BD confirmed through a recent evaluation of BD BBL™ Sensi-Disc™ product that twenty-eight (28) out of thirty (30) antimicrobial discs showed reproducibility, accuracy, and/or quality control (qc) failures when tested with Haemophilus spp. Testing with other bacterial pathogens (where indicated) is not affected.

Recall Start Date: December 29, 2023

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Microbiology
Companies

Becton Dickinson And Company (BD)

7 Loveton Circle, Sparks, Maryland, United States, 21152

Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-74891

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