# China NMPA Product Recall - Trauma surgical instrument kit, orthopedic drill bits

Source: https://www.globalkeysolutions.net/records/china_product_recall/synthes-gmbh/22e2a0ae-f42e-4421-9654-fe5d07c95919/
Source feed: China

> China NMPA product recall for Trauma surgical instrument kit, orthopedic drill bits by Synthes GmbH published January 11, 2017. Recall level: . The National Medical Products Administration (NMPA) announced a voluntary product recall initiated b

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Synthes GmbH recalls trauma surgical instrument kits and orthopedic drills.
- Company Name: Synthes GmbH
- Publication Date: 2017-01-11
- Product Name: Trauma surgical instrument kit, orthopedic drill bits
- Recall Reason: The flexible shaft (352.040) and movable extension rod (352.044) of the trauma surgical instrument kit in the affected batch may have been made with an asymmetrical hexagonal coupler, resulting in different lengths of each side of the hexagon and the center of the hexagon not being located on the center line. This may cause the flexible shaft to be mismatched with the tip of the reamer it is nested in.
- Discovering Company: Johnson & Johnson (Shanghai) Medical Devices Co., Ltd.
- Manufacturing Company: Synthes GmbH
- Summary: The National Medical Products Administration (NMPA) announced a voluntary product recall initiated by Synthes GmbH, involving specific trauma surgical instrument kits and orthopedic drills, distributed by Johnson & Johnson (Shanghai) Medical Devices Co., Ltd. The recall, formally reported in February 2016 and published by NMPA in January 2017, addresses a manufacturing flaw in the flexible shaft (model 352.040) and movable extension rod (model 352.044) components. These parts were found to have asymmetrical hexagonal couplers, leading to inconsistent side lengths and an off-center connection point. This defect could prevent the flexible shaft from properly engaging with the head of its nested reamer.

Synthes GmbH initiated the recall under the NMPA’s regulatory framework for medical devices. Critically, the manufacturer confirmed that no affected batches of these products were imported or sold within mainland China. Therefore, no direct corrective actions were mandated for the Chinese market. However, the NMPA requested all provincial and autonomous region drug administrations to strengthen their supervision and management of similar medical devices to proactively ensure compliance and public safety. The recall did impact several international markets, including the United States, Japan, and European countries.

Company: https://www.globalkeysolutions.net/companies/synthes-gmbh/77a06946-ba7a-4bf2-916a-600eabfb0ce7/