# China NMPA Product Recall - Polypectomy Snare

Source: https://www.globalkeysolutions.net/records/china_product_recall/wilson-cook-medical-incorporated/218fbb1a-fe2b-4699-b014-cdc17d3eb094/
Source feed: China

> China NMPA product recall for Polypectomy Snare by Wilson-Cook Medical Incorporated published February 05, 2024. Recall level: Level 3 Recall. Wilson-Cook Medical Incorporated, in conjunction with its subsidiary Cook (China) Medical Trading Co

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Wilson-Cook Medical Incorporated is voluntarily recalling its polyp removal device.
- Company Name: Wilson-Cook Medical Incorporated
- Publication Date: 2024-02-05
- Product Name: Polypectomy Snare
- Recall Level: Level 3 Recall
- Recall Reason: The label model information for a specific batch of products is incorrect.
- Discovering Company: Cook (China) Medical Trading Co., Ltd.
- Manufacturing Company: Wilson-Cook Medical Incorporated
- Summary: Wilson-Cook Medical Incorporated, in conjunction with its subsidiary Cook (China) Medical Trading Co., Ltd., has initiated a voluntary Class III recall of its Polypectomy Snare. This action was officially announced by the National Medical Products Administration (NMPA) on February 5, 2024. The recall is a direct response to the discovery of incorrect labeling information pertaining to a specific batch of the medical device. The Polypectomy Snare, identified by National Medical Device Registration Certificate 20153014006, is being recalled proactively by the manufacturer to rectify the labeling discrepancy. While the document does not mention specific inspection dates, the company's prompt, voluntary recall demonstrates adherence to regulatory responsibilities under the NMPA framework. The main issue is a critical error in product labeling rather than a functional defect of the device itself. A Class III recall indicates that the use of or exposure to the affected product is not likely to cause adverse health consequences. Wilson-Cook Medical Incorporated's required action involves retrieving the impacted products to ensure full compliance and uphold patient safety standards. Detailed information concerning the specific affected product models, specifications, and batch numbers is available in the associated "Medical Device Recall Event Report Form."

Company: https://www.globalkeysolutions.net/companies/wilson-cook-medical-incorporated/231fac5e-c806-491e-868c-7ad3be8c12fa/