# China NMPA Product Recall - Groshong NXT PICC Catheter Kit and Accessories

Source: https://www.globalkeysolutions.net/records/china_product_recall/bard-medical-technology-shanghai-co-ltd/2e8a487d-047a-4cf7-9c6b-e073d8b59677/
Source feed: China

> China NMPA product recall for Groshong NXT PICC Catheter Kit and Accessories by Bard Medical Technology (Shanghai) Co., Ltd. published July 13, 2021. Recall level: Level 2 Recall. Bard Medical Technology (Shanghai) Co., Ltd. initiated a voluntary Class II recall of its Groshong N

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Bard Medical Technology (Shanghai) Co., Ltd. is voluntarily recalling its peripherally inserted central venous catheter kit and accessory, Groshong NXT PICC Catheter.
- Company Name: Bard Medical Technology (Shanghai) Co., Ltd.
- Publication Date: 2021-07-13
- Product Name: Groshong NXT PICC Catheter Kit and Accessories
- Recall Level: Level 2 Recall
- Recall Reason: Some batches of "Peripherally Inserted Central Venous Catheter Kits and Accessories" products may have external connectors that fail to lock into place upon initial connection.
- Discovering Company: Bard Medical Technology (Shanghai) Co., Ltd.
- Manufacturing Company: Bard Medical Technology (Shanghai) Co., Ltd.
- Summary: Bard Medical Technology (Shanghai) Co., Ltd. initiated a voluntary Class II recall of its Groshong NXT PICC Catheter Kits and accessories, as announced on July 13, 2021. This action, overseen by the National Medical Products Administration (NMPA) in China, addresses a discovered issue where external connectors on certain batches of these Peripherally Inserted Central Venous Catheter Kits and Accessories may fail to lock securely upon initial connection. The problem was first identified in the U.S. The company has not received reports of serious adverse events related to this specific issue in China. As required actions, Bard Medical Technology (Shanghai) Co., Ltd. will inform customers about procedures for handling these abnormalities and provide necessary replacement parts. The recall pertains to products under Registration Certificate No.: 20173771671, with specific details on affected models and batches provided in the Medical Device Recall Event Report Form.

Company: https://www.globalkeysolutions.net/companies/bard-medical-technology-shanghai-co-ltd/4bdd60c0-a2ea-4471-a538-4d3b6da1fcac/