China NMPA Product Recall - Kendall SCD 700 Sequential Compression System (Intermittent Pneumatic Pressure Equipment)

Cardinal Health 200, LLC has initiated a voluntary Level III recall of its Kendall SCD 700 Sequential Compression System. This action, reported by Cardinal Health (Shanghai) Medical Devices Co., Ltd., addresses potential safety risks arising from the use of non-original power cords with the device. The recall pertains to products registered under National Medical Device Registration Certificate No. 20242090177, overseen by the National Medical Products Administration (NMPA). The decision to recall was made to safeguard patient and user safety by mitigating risks associated with incompatible power accessories. While specific inspection dates are not detailed in this announcement, the recall itself serves as a crucial regulatory response to identified product safety concerns. Affected models, specifications, and specific product batches are thoroughly outlined in the comprehensive "Medical Device Recall Event Report Form" attached to the official NMPA notice. This proactive measure by Cardinal Health aims to ensure compliance with medical device safety standards and protect public health. Customers and healthcare providers are advised to refer to the detailed report for guidance on identifying and handling affected devices.