# China NMPA Product Recall - Transparent pinless connector

Source: https://www.globalkeysolutions.net/records/china_product_recall/kangerfusheng-shanghai-trading-co-ltd/35b0364a-8d6d-4f24-bcce-47873dcb442c/
Source feed: China

> China NMPA product recall for Transparent pinless connector by Kangerfusheng (Shanghai) Trading Co., Ltd. published May 07, 2019. Recall level: Level 2. Kangfusheng (Shanghai) Trading Co., Ltd. initiated a voluntary Class II recall of its transparent ne

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Kangerfusheng (Shanghai) Trading Co., Ltd. is voluntarily recalling its transparent pinless connectors.
- Company Name: Kangerfusheng (Shanghai) Trading Co., Ltd.
- Publication Date: 2019-05-07
- Product Name: Transparent pinless connector
- Recall Level: Level 2
- Recall Reason: After the transparent positive pressure needleless connector is disconnected, tiny droplets may form on the connector surface. These droplets could come into contact with healthcare professionals, patients, or the surrounding area, posing a potential risk.
- Discovering Company: Kangerfusheng (Shanghai) Trading Co., Ltd.
- Manufacturing Company: Kangerfusheng (Shanghai) Trading Co., Ltd.
- Summary: Kangfusheng (Shanghai) Trading Co., Ltd. initiated a voluntary Class II recall of its transparent needleless connectors, as announced by the National Medical Products Administration (NMPA) on May 7, 2019. The Shanghai Food and Drug Administration's medical device registration certificate number associated with the recall is 2019-104, while the product's registration certificate number is 20153661152. The primary issue identified is the formation of tiny droplets on the connector surface after disconnection. These droplets present a potential risk by possibly contacting healthcare professionals, patients, or the surrounding environment. In response, Kangfusheng (Shanghai) Trading Co., Ltd. is undertaking the recall to address this safety concern. Specific details regarding the affected product models, specifications, and batch numbers are provided in the "Medical Device Recall Event Report Form," which accompanies the NMPA's public announcement. The recall emphasizes the company's proactive measure to mitigate potential health risks associated with the product.

Company: https://www.globalkeysolutions.net/companies/kangerfusheng-shanghai-trading-co-ltd/81df839f-c323-45be-b17a-ccd9dd6d1dfc/