# China NMPA Product Recall - Instrum Trauma Surgery Surgical Instrument Kit

Source: https://www.globalkeysolutions.net/records/china_product_recall/synthes-gmbh/4def4414-e07a-491f-8134-d6ef00c4fd7b/
Source feed: China

> China NMPA product recall for Instrum Trauma Surgery Surgical Instrument Kit by Synthes GmbH published May 08, 2024. Recall level: Level 3 Recall. Synthes GmbH, a medical device manufacturer, has initiated a voluntary Class III recall for its Inst

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Synthes GmbH is voluntarily recalling trauma surgical instrument kits.
- Company Name: Synthes GmbH
- Publication Date: 2024-05-08
- Product Name: Instrum Trauma Surgery Surgical Instrument Kit
- Recall Level: Level 3 Recall
- Recall Reason: The groove at the top of the screwdriver shaft was not machined.
- Discovering Company: Johnson & Johnson (Shanghai) Medical Devices Co., Ltd.
- Manufacturing Company: Synthes GmbH
- Summary: Synthes GmbH, a medical device manufacturer, has initiated a voluntary Class III recall for its Instrum Trauma Surgical Instrument Kit. This significant action was reported to the National Medical Products Administration (NMPA) on May 8, 2024, by Johnson & Johnson (Shanghai) Medical Devices Co., Ltd., the product's distributor. The core issue driving this recall is a manufacturing defect: an unfinished groove at the tip of a screwdriver shaft contained within the surgical kits.

While the document does not specify inspection dates, the recall is a proactive measure undertaken by Synthes GmbH to address this product deficiency. The Class III designation indicates that the identified issue is considered unlikely to cause serious adverse health consequences but still warrants corrective action to maintain product quality and safety standards. This recall operates within the regulatory framework established by the NMPA, which oversees medical device safety and compliance in China.

As part of the required actions, Johnson & Johnson (Shanghai) Medical Devices Co., Ltd. has formally reported the event, providing essential details about the affected product models, specifications, and batch numbers in a "Medical Device Recall Event Report Form." This comprehensive documentation ensures transparency and facilitates the efficient retrieval of all impacted devices from the market, upholding regulatory expectations and commitment to patient well-being.

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