China NMPA Product Recall - T2 Nailing Systems

Stryker GmbH is voluntarily recalling its T2 Nailing Systems, as reported by Stryker (Beijing) Medical Devices Co., Ltd. The recall, classified as Class III by the National Medical Products Administration (NMPA), stems from significant discrepancies identified between the product information displayed on the packaging labels and the actual products themselves. This issue pertains to products registered under National Medical Device Registration Certificate No. 20163132780. The recall was announced on June 11, 2025. It is crucial to note that the specific products subject to this recall were not imported into China. Detailed information regarding affected models, specifications, and batches is available in the “Medical Device Recall List” and the attached “Medical Device Recall Event Report Form” from Stryker AG. The NMPA oversees this regulatory action, ensuring product safety and compliance within its jurisdiction.