# China NMPA Product Recall - Jet-X external fixator instrument system

Source: https://www.globalkeysolutions.net/records/china_product_recall/smith-nephew-inc/ab0b5549-fa3c-4afc-a3a0-e49f4e62121a/
Source feed: China

> China NMPA product recall for Jet-X external fixator instrument system by Smith & Nephew Inc. published December 30, 2021. Recall level: Level 3 Recall. On December 30, 2021, the National Medical Products Administration (NMPA) announced a voluntary Clas

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Smith & Nephew, Inc. Jet-X external fixator instrument system proactive recall.
- Company Name: Smith & Nephew Inc.
- Publication Date: 2021-12-30
- Product Name: Jet-X external fixator instrument system
- Recall Level: Level 3 Recall
- Recall Reason: The gasket of the locking needle pressure unit was made of the wrong plastic material, which may crack during autoclaving, causing the pressure unit to malfunction.
- Discovering Company: Smith & Nephew Medical Products International Trading (Shanghai) Co., Ltd.
- Manufacturing Company: Smith & Nephew Inc.
- Summary: On December 30, 2021, the National Medical Products Administration (NMPA) announced a voluntary Class III recall initiated by Smith & Nephew, Inc., specifically involving its Jet-X External Fixator Instrument System. This recall was prompted by Smith & Nephew Medical Products International Trading (Shanghai) Co., Ltd. reporting a critical issue with certain models and batches of the product. The primary concern identified was the use of an incorrect plastic material for the gasket within the locking needle pressure device. This material defect poses a significant risk, as it may cause the gasket to crack when subjected to autoclaving sterilization procedures. Such cracking could lead directly to a malfunction of the pressure device, potentially compromising the safety and efficacy of the external fixator system during medical use. The recall, overseen by the NMPA, requires the removal of all affected units from the market. Comprehensive details regarding the specific models, specifications, and batch numbers implicated in this recall are provided in the associated Medical Device Recall Event Report Form, ensuring stakeholders can accurately identify and manage affected products. This action underscores the manufacturer's commitment, under NMPA's regulatory oversight, to patient safety and product integrity.

Company: https://www.globalkeysolutions.net/companies/smith-nephew-inc/feb94bf5-8eb9-4a12-b2f7-02767ea39056/