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

Source: https://www.globalkeysolutions.net/records/china_product_recall/synthes-gmbh/c0ae4dac-1011-4f14-9633-fa5e15b507ce/
Source feed: China

> China NMPA product recall for Trauma surgical instrument kit and orthopedic drill by Synthes GmbH published January 11, 2017. Recall level: . The National Medical Products Administration (NMPA) issued an advisory on January 11, 2017, concerni

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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 and orthopedic drill
- 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) issued an advisory on January 11, 2017, concerning a voluntary recall initiated by medical device manufacturer Synthes GmbH. This recall, reported by its distributor, Johnson & Johnson (Shanghai) Medical Devices Co., Ltd. on January 21, 2016, impacts specific batches of Trauma Surgical Instrument Kits (Model 352.040) and Orthopedic Drills (Model 352.044). The core issue stems from a manufacturing defect: the flexible shaft of the trauma kits and the movable extension rod of the orthopedic drills may have an asymmetrical hexagonal coupler. This structural flaw could lead to uneven hexagonal side lengths, causing the flexible shaft to improperly mate with its corresponding reamer head, thereby compromising the devices' functionality. While this Class I medical device recall extended to numerous countries, including the United States and Germany, Johnson & Johnson affirmed that none of the affected products were imported into or sold within China. Therefore, no direct corrective actions were mandated for the Chinese market. However, the NMPA directed provincial and municipal food and drug administrations to reinforce their supervisory and management efforts over similar medical products to safeguard public health and ensure compliance with regulatory standards.

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