# China NMPA Product Recall - Laparoscopic articular head linear cutting stapler and staple cartridge, electric laparoscopic linear cutting stapler and staple cartridge

Source: https://www.globalkeysolutions.net/records/china_product_recall/ethicon-endo-surgery-llc/3da1c047-15c3-4a25-94a0-5f9bc36f664c/
Source feed: China

> China NMPA product recall for Laparoscopic articular head linear cutting stapler and staple cartridge, electric laparoscopic linear cutting stapler and staple cartridge by Ethicon Endo-Surgery, LLC published November 18, 2019. Recall level: Level 2 Recall. The National Medical Products Administration (NMPA) published an index concerning a voluntary produc

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Ethicon Endo-Surgery, LLC is proactively recalling its laparoscopic arthroscopic linear stapler and cartridge, as well as its motorized laparoscopic linear stapler and cartridge.
- Company Name: Ethicon Endo-Surgery, LLC
- Publication Date: 2019-11-18
- Product Name: Laparoscopic articular head linear cutting stapler and staple cartridge, electric laparoscopic linear cutting stapler and staple cartridge
- Recall Level: Level 2 Recall
- Recall Reason: Some products may contain non-compliant anvils within the jaws, causing staple deformation and affecting the integrity of the linear fit.
- Discovering Company: Johnson & Johnson (Shanghai) Medical Devices Co., Ltd.
- Manufacturing Company: Ethicon Endo-Surgery, LLC
- Summary: The National Medical Products Administration (NMPA) published an index concerning a voluntary product recall initiated by Ethicon Endo-Surgery, LLC, the manufacturer. This recall, referenced under NMPA Index No. JGXX-2019-10767, specifically targets laparoscopic arthroscopic linear cutting staplers and staple cartridges, alongside motorized laparoscopic linear cutting staplers and staple cartridges. The primary issue, identified and reported by Johnson & Johnson (Shanghai) Medical Devices Co., Ltd., involves a manufacturing defect where some of these surgical devices may contain non-compliant anvils within their jaws. This critical flaw can result in staple deformation during use, thereby compromising the intended integrity of linear anastomosis in surgical applications. The NMPA classified this as a Level II active device recall. This classification signifies that while the use of or exposure to the affected products may cause temporary or medically reversible adverse health consequences, the probability of serious adverse health consequences is considered remote. As part of this required action, Ethicon Endo-Surgery, LLC is voluntarily removing these products from the market. Comprehensive details, including the specific models, specifications, and affected product batches, are provided in the accompanying 'Medical Device Recall Event Report Form,' ensuring transparency and facilitating the recall process in adherence to regulatory requirements.

Company: https://www.globalkeysolutions.net/companies/ethicon-endo-surgery-llc/dfce5be3-6a9d-4239-8ba0-5d5283b81a02/