# China NMPA Product Recall - Endoscopic surgical manual tools

Source: https://www.keypedia.com/records/china_product_recall/smith-nephew-inc/5d3ae14b-2be5-4070-a267-3b94c4250ed1
Source feed: China

> China NMPA product recall for Endoscopic surgical manual tools by Smith & Nephew Inc. published May 07, 2015. Recall level: Level II. On May 7, 2015, the National Medical Products Administration (NMPA) announced a Class II voluntary r

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Smith & Nephew Medical Products International Trading (Shanghai) Co., Ltd. is voluntarily recalling manual instruments for endoscopic surgery.
- Company Name: Smith & Nephew Inc.
- Publication Date: 2015-05-07
- Product Name: Endoscopic surgical manual tools
- Recall Level: Level II
- Recall Reason: Smith & Nephew's internal investigation found that the product's packaging materials and design may not have been able to prevent the product's sharp edges from puncturing the sterilization packaging, thus preventing the product from maintaining a sterile state.
- Discovering Company: Smith & Nephew Medical Products International Trading (Shanghai) Co., Ltd.
- Manufacturing Company: Smith & Nephew Inc.
- Summary: On May 7, 2015, the National Medical Products Administration (NMPA) announced a Class II voluntary recall initiated by Smith & Nephew Medical Products International Trading (Shanghai) Co., Ltd., on behalf of its manufacturer, Smith & Nephew Inc. The recall targeted specific batches of Manual Endoscopic Surgical Tools (Product Number 72201537, manufactured between April 2010 and April 2014). The critical issue, identified during Smith & Nephew's internal investigation, was a design flaw in the product's packaging. It was determined that the sharp edges of the surgical tools could potentially puncture the sterilization packaging, leading to a loss of product sterility and posing a significant risk during medical procedures. To address this, Smith & Nephew initiated a global recall. Required actions included the Sales Department distributing recall notices to affected distributors, who were then responsible for notifying subsequent partners and hospitals. The Supply Chain Department oversaw the retrieval of all affected products to a Shanghai warehouse, facilitating their return to the U.S. manufacturing facility for processing. Furthermore, distributors received refunds or exchanges for the returned items. This proactive measure was taken to ensure patient safety by preventing the use of potentially non-sterile surgical instruments.

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