BD Initiates Class II Recall of Mycobacteria Streptomycin Susceptibility Test Kit Due to Label Expiry Date Error
BD
Medical Device R&D Manufacturer, Distributor
Recently, Diagnostic Science learned from the National Medical Products Administration (NMPA),1 IVD ProductInitiate recall, details as follows:
Company Name:Becton, Dickinson and Company
Product Name:Mycobacterium Tuberculosis Streptomycin Susceptibility Kit (Fluorescence Method) BD BACTEC™ MGIT™ 960 STR 4.0 Kit
Product Certificate Number:China Medical Device Registration No. 20152400309
Recall Level:Level 2 Recall
Recall Date:October 22, 2025
Reason for Recall:Due to BD's discovery of an error in the expiration date on the label of the streptomycin solution vial in a specific batch of mycobacterial streptomycin susceptibility test kits.
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