# China NMPA Product Recall - TRUCLEAR Hysteroscopic Morcellator

Source: https://www.globalkeysolutions.net/records/china_product_recall/smith-nephew-inc/02f73ebf-5615-4378-a64b-8da7baa6ff1c/
Source feed: China

> China NMPA product recall for TRUCLEAR Hysteroscopic Morcellator by Smith & Nephew Inc. published August 10, 2022. Recall level: Level 2 Recall. The National Medical Products Administration (NMPA) has announced a Level II voluntary recall of the

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Smith & Nephew Inc. is voluntarily recalling its TRUCLEAR Hysteroscopic Morcellator.
- Company Name: Smith & Nephew Inc.
- Publication Date: 2022-08-10
- Product Name: TRUCLEAR Hysteroscopic Morcellator
- Recall Level: Level 2 Recall
- Recall Reason: In certain models and batches of products, when the foot switch and handle are used simultaneously, an error code E6 will illuminate on the control unit's red indicator light, causing the device to malfunction.
- Discovering Company: Covidien Medical Devices International Trading (Shanghai) Co., Ltd.
- Manufacturing Company: Smith & Nephew Inc.
- Summary: The National Medical Products Administration (NMPA) has announced a Level II voluntary recall of the TRUCLEAR Hysteroscopic Morcellator, manufactured by Smith & Nephew Inc. The recall, reported by Covidien Medical Devices International Trading (Shanghai) Co., Ltd. and published on August 10, 2022, addresses a critical functionality issue. Specifically, certain models and batches of the device (Registration Certificate No.: 20173547251) exhibit a red indicator light and generate error code E6 when the foot switch and handle are activated concurrently. This operational flaw renders the device inoperable during use, which could potentially disrupt surgical procedures and impact patient care. Smith & Nephew Inc. initiated this recall to address the performance deficiency and ensure the safety and reliability of their medical devices. The Level II classification indicates that the product defect may cause temporary or reversible adverse health consequences, or that the probability of serious adverse health consequences is remote. Comprehensive details concerning the specific affected product models, specifications, and batch numbers are provided in the accompanying 'Medical Device Recall Event Report Form.' This action highlights the regulatory responsibility under the NMPA to oversee medical device quality and prompt manufacturers to rectify issues that could compromise patient safety or clinical outcomes.

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