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Becton Dickinson & Co. Recall 93789

Description: BD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231691 and 231692¿

Becton Dickinson & Co. Recall 93789 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1037-2024
Event ID93789
Event DescriptionBD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231691 and 231692¿
Product TypeDevices
DistributionDomestic distribution nationwide. International distribution worldwide.
Quantity2,363,168 total units
Recall ReasonThere is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or additional adverse diagnostic outcomes, such as a delay in diagnosis, the selection of inappropriate antibiotics, or extended duration of antibiotic exposure and the treatment process.
Device Classification20240214
Device Code InfoCatalog No. 231691 UDI-DI 00382902316916 Lots 1301719 2026369 2056587 2119595 3003951 3062107 3118199 3275730; Catalog No. 231692¿ UDI-DI 30382902316924 Lots 3003951 3184117 3223408 3275730 1301719 2026369 2056587 2119595 2147716 2244463 3062107 3118199
Center Classification Date20240208
Recall Initiation Date20240108
Recalling FirmBecton Dickinson & Co.
Initial Notification Letter
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