# China NMPA Product Recall - Disposable dialysis blood circuit tubing

Source: https://www.globalkeysolutions.net/records/china_product_recall/jiangsu-fresenius-medical-supplies-co-ltd/77e33799-74de-4aa8-ba49-db01eaa1a901/
Source feed: China

> China NMPA product recall for Disposable dialysis blood circuit tubing by Jiangsu Fresenius Medical Supplies Co., Ltd. published October 12, 2017. Recall level: Level 3 Recall. Jiangsu Fresenius Medical Supplies Co., Ltd. announced a voluntary Class III recall of its disposabl

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Jiangsu Fresenius Medical Supplies Co., Ltd. voluntarily recalls disposable dialysis blood circuit tubing.
- Company Name: Jiangsu Fresenius Medical Supplies Co., Ltd.
- Publication Date: 2017-10-12
- Product Name: Disposable dialysis blood circuit tubing
- Recall Level: Level 3 Recall
- Recall Reason: The clip may have a potential closure issue.
- Discovering Company: Jiangsu Fresenius Medical Supplies Co., Ltd.
- Manufacturing Company: Jiangsu Fresenius Medical Supplies Co., Ltd.
- Summary: Jiangsu Fresenius Medical Supplies Co., Ltd. announced a voluntary Class III recall of its disposable dialysis blood circuit tubes, publicly reported on October 12, 2017. The primary reason for this recall is a potential closure problem associated with the clips of these medical devices. Specific dates of inspection leading to this discovery were not detailed in the public notice; however, the company proactively reported the issue concerning products identified by CFDA registration numbers 20133451346 and 20173450509. This corrective action falls under the regulatory oversight of the National Medical Products Administration (NMPA) and reflects the company's responsibility to manage product quality and patient safety within the medical device industry. A Class III recall typically signifies that the product defect has a low probability of causing serious adverse health consequences but still necessitates withdrawal from the market to maintain quality standards and prevent potential future risks. The required action involves the removal of the affected devices from circulation. Comprehensive details regarding the specific models, specifications, and batch numbers impacted by this recall are provided in the company's official "Medical Device Recall Event Report Form," ensuring transparency and enabling proper remediation by healthcare providers and distributors.

Company: https://www.globalkeysolutions.net/companies/jiangsu-fresenius-medical-supplies-co-ltd/218e6a25-7b73-434e-902e-63654a76a82d/