BD Kiestra B.V. Initiates Class II Recall of BD Kiestra™ InoqulA+™ TLA Automated Microbiology Sample Processing System Due to Software Issue

Website of the National Medical Products Administration, April 23rd: Becton Dickinson Medical Devices (SHANGHAI) Co., Ltd. reported that due to a software issue that may lead to incorrect information processing, the manufacturer BD Kiestra B.V. voluntarily recalled the fully automatic microbial sample processing system BD Kiestra™ InoqulA+™ TLA (Record No. 20220143). The recall level is Class II.