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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