# China NMPA Product Recall - Floating tube

Source: https://www.globalkeysolutions.net/records/china_product_recall/edwards-lifesciences-llc/211e7778-d0b8-460f-83ee-a12f57f471f3/
Source feed: China

> China NMPA product recall for Floating tube by Edwards Lifesciences LLC published July 14, 2023. Recall level: Level 3 Recall. Edwards Lifesciences LLC, a prominent medical device manufacturer, initiated a voluntary Class III r

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Edwards Lifesciences LLC is voluntarily recalling its floating catheters.
- Company Name: Edwards Lifesciences LLC
- Publication Date: 2023-07-14
- Product Name: Floating tube
- Recall Level: Level 3 Recall
- Recall Reason: There is an issue with updating the labeling of certain product models.
- Discovering Company: Edwards (Shanghai) Medical Supplies Co., Ltd.
- Manufacturing Company: Edwards Lifesciences LLC
- Summary: Edwards Lifesciences LLC, a prominent medical device manufacturer, initiated a voluntary Class III recall for specific models of its floating catheters, as announced on July 14, 2023. This action was officially reported by its affiliate, Edward (Shanghai) Medical Supplies Co., Ltd., to the National Medical Products Administration (NMPA) of China. The central reason for this recall stems from an identified labeling update issue concerning the affected products. While no inspection dates are provided, the voluntary nature of the recall underscores the company's proactive commitment to addressing product discrepancies. The recall specifically pertains to devices registered under Medical Device Registration Certificate No. 20163074711. The regulatory oversight for this recall falls under the NMPA, which governs medical device safety and quality standards in China. A Class III recall indicates that the use of or exposure to the product is unlikely to cause adverse health consequences. As part of the required actions, Edwards Lifesciences LLC is systematically removing the impacted floating catheters from distribution. Comprehensive details regarding the precise models, specifications, and batch numbers affected by this recall are formally documented in the accompanying "Medical Device Recall Event Report Form," ensuring full transparency and facilitating the effective execution of the recall process to uphold patient safety and regulatory compliance.

Company: https://www.globalkeysolutions.net/companies/edwards-lifesciences-llc/d78876e8-6a4a-49b4-8cb5-30579a7ed097/