# China NMPA Product Recall - Endoscopic surgical manual tools

Source: https://www.globalkeysolutions.net/records/china_product_recall/smith-nephew-inc-endoscopy-division/50265e26-3ca6-4b2a-a771-cdb24c85a213/
Source feed: China

> China NMPA product recall for Endoscopic surgical manual tools by Smith & Nephew, Inc. Endoscopy Division published August 18, 2020. Recall level: Level 2 Recall. Smith & Nephew Inc. Endoscopy Division initiated a voluntary recall of its manual endoscopic surgica

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Smith & Nephew Inc. Endoscopy Division is voluntarily recalling manual endoscopic surgical instruments.
- Company Name: Smith & Nephew, Inc. Endoscopy Division
- Publication Date: 2020-08-18
- Product Name: Endoscopic surgical manual tools
- Recall Level: Level 2 Recall
- Recall Reason: The packaging of a specific model or batch of products was incorrect, resulting in a discrepancy between the product displayed on the outer packaging and the actual product.
- Discovering Company: Smith & Nephew Medical Products International Trading (Shanghai) Co., Ltd.
- Manufacturing Company: Smith & Nephew, Inc. Endoscopy Division
- Summary: Smith & Nephew Inc. Endoscopy Division initiated a voluntary recall of its manual endoscopic surgical tools, publicly announced on August 18, 2020. This action, conducted in cooperation with its subsidiary Smith & Nephew Medical Products International Trading (Shanghai) Co., Ltd., stemmed from packaging errors. The core issue involved the outer packaging of specific product models and batches not accurately matching the actual medical devices inside. Overseen by the National Medical Products Administration (NMPA) in China, this recall was designated as Class II. While the document does not specify inspection dates, the voluntary recall itself signifies the company's commitment to product safety. The company proactively chose to remove the affected products from the market to prevent potential issues arising from mislabeled packaging. Further detailed information on the precise models and batches impacted by this discrepancy is available in the accompanying "Medical Device Recall Event Report Form." This action underscores Smith & Nephew's adherence to regulatory standards and its dedication to ensuring product quality and patient safety.

Company: https://www.globalkeysolutions.net/companies/smith-nephew-inc-endoscopy-division/df034cb9-0899-4c11-a410-b8102d0e5fec/