Public recall detail

BBL Sensi-Disc Antimicrobial Susceptibility Test Discs

2024-01-10

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Recall Safety notice
Quick summary

Quick summary: BBL Sensi-Disc Antimicrobial Susceptibility Test Discs. Date: 2024-01-10.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: BBL Sensi-Disc Antimicrobial Susceptibility Test Discs. Date: 2024-01-10.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandBecton Dickinson And Company [Bd]
ProductBBL Sensi-Disc Antimicrobial Susceptibility Test Discs
IssueMedical devices - Device compatibility
Recall classType II
IdentificationRA-74891

Affected products

ProductBBL Sensi-Disc Antimicrobial Susceptibility Test Discs
LotMore than 10 numbers, contact manufacturer.
Model203705 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
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionBBL Sensi-Disc Antimicrobial Susceptibility Test Discs
ProductBBL Sensi-Disc Antimicrobial Susceptibility Test Discs
LotMore than 10 numbers, contact manufacturer.
Model231658 231664 231692 231758 232175 230998 231633 231678 231691 231536 231539 231621 231632 231660 231672 231704 232219 232231
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionBBL Sensi-Disc Antimicrobial Susceptibility Test Discs

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

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Healthcare Industry
CategoryHealth products - Medical devices - Microbiology
CompaniesBecton Dickinson And Company (BD) 7 Loveton Circle, Sparks, Maryland, United States, 21152
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-74891
Background{}
CompaniesBecton Dickinson And Company (BD) 7 Loveton Circle, Sparks, Maryland, United States, 21152
AudiencesGeneral public Healthcare Industry
Source updated2024-01-10

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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