# China NMPA Product Recall - Percutaneous sheath puncture group, central venous catheter kit

Source: https://www.globalkeysolutions.net/records/china_product_recall/arrow-international-inc/ad11e261-1db2-4915-a164-6a8a0f6bf619
Source feed: China

> China NMPA product recall for Percutaneous sheath puncture group, central venous catheter kit by Arrow International Inc. published May 06, 2022. Recall level: Level 3 Recall. Arrow International LLC initiated a voluntary recall for Percutaneous Catheterization Kits, Central 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Arrow International LLC is voluntarily recalling products including percutaneous sheathing kits and central venous catheter kits.
- Company Name: Arrow International Inc.
- Publication Date: 2022-05-06
- Product Name: Percutaneous sheath puncture group, central venous catheter kit
- Recall Level: Level 3 Recall
- Recall Reason: The needle hub cracked due to pressure during catheterization.
- Discovering Company: Telif Medical Devices Trading (Shanghai) Co., Ltd.
- Manufacturing Company: Arrow International Inc.
- Summary: Arrow International LLC initiated a voluntary recall for Percutaneous Catheterization Kits, Central Venous Catheter Kits, and other related products. This action was publicly reported on May 6, 2022, by Telefel Medical Devices Trading (Shanghai) Co., Ltd., in an announcement overseen by China's National Medical Products Administration (NMPA). The core issue prompting the recall is a potential defect where the needle hub may crack under pressure during catheterization procedures, posing a concern for product reliability and patient safety. Operating under NMPA's regulatory framework, the recall has been designated as Class III. The required action involves the voluntary withdrawal of specific models and batches of the affected medical devices from the market. Detailed information regarding the precise products involved, including their registration numbers, models, specifications, and batch identifiers, is available in a supplementary "Medical Device Recall Event Report Form." This proactive measure by Arrow International LLC demonstrates a commitment to upholding product quality and ensuring patient safety within the medical device sector.

Company: https://www.globalkeysolutions.net/companies/arrow-international-inc/8820e141-5ce7-4e2d-844a-672ff4232c9c