# China NMPA Product Recall - Thru-Lumen Embolectomy Catheter

Source: https://www.globalkeysolutions.net/records/china_product_recall/edwards-lifesciences-llc/00e0762c-4ff2-47b3-a9f3-04b81e2b6e12/
Source feed: China

> China NMPA product recall for Thru-Lumen Embolectomy Catheter by Edwards Lifesciences LLC published September 06, 2023. Recall level: Level 2 Recall. On September 6, 2023, Edwards Lifesciences LLC initiated a voluntary Class II recall for its Thru-Lu

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Edwards Lifesciences LLC is voluntarily recalling its dual-lumen thrombectomy catheter.
- Company Name: Edwards Lifesciences LLC
- Publication Date: 2023-09-06
- Product Name: Thru-Lumen Embolectomy Catheter
- Recall Level: Level 2 Recall
- Recall Reason: Certain batches of products may have a lower balloon deflation rate than normal.
- Discovering Company: Edwards (Shanghai) Medical Supplies Co., Ltd.
- Manufacturing Company: Edwards Lifesciences LLC
- Summary: On September 6, 2023, Edwards Lifesciences LLC initiated a voluntary Class II recall for its Thru-Lumen Embolectomy Catheter, a critical medical device. This action was officially reported by Edwards (Shanghai) Medical Supplies Co., Ltd. and is overseen by the National Medical Products Administration (NMPA) in China. The core issue precipitating this recall is the discovery of a potential lower-than-normal balloon deflation rate in specific manufacturing batches of the catheter. Such a malfunction could significantly impact the device's performance during embolectomy procedures, potentially leading to complications or adverse patient outcomes if the balloon does not deflate as intended. The affected product is identified by National Medical Device Registration Certificate No. 20163030176. Although the document does not specify inspection dates, the recall date signifies the company's prompt response to a potential quality control issue. Edwards Lifesciences LLC is undertaking this voluntary recall as a necessary measure to ensure patient safety and maintain product efficacy. Detailed information regarding the precise models, specifications, and batch numbers involved is contained within the "Recall Event Report Form." This proactive step demonstrates adherence to regulatory standards and a commitment to addressing product deficiencies to safeguard public health.

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