Becton, Dickinson and Company Initiates Class II Voluntary Recall of BD BACTEC™ MGIT™ 960 STR 4.0 Kit Due to Incorrect Expiration Date on Streptomycin Vial Labels

Source: Website of the National Medical Products Administration

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, the manufacturer Becton, Dickinson and Company initiated a voluntary recall of its BD BACTEC™ MGIT™ 960 STR 4.0 Kit (fluorescence method) for mycobacterial streptomycin susceptibility testing (Registration No.: 20152400309 Imported Medical Device Registration in China). The recall is classified as a Level II recall. Detailed information regarding the models, specifications, and batches of the affected products can be found in the Medical Device Recall Report.