# China NMPA Product Recall - Diffused braided artificial blood vessels

Source: https://www.globalkeysolutions.net/records/china_product_recall/maikewei-shanghai-medical-equipment-co-ltd/cd9c6168-54a5-4ea4-b22b-704aa446eb46/
Source feed: China

> China NMPA product recall for Diffused braided artificial blood vessels by Maikewei (Shanghai) Medical Equipment Co., Ltd. published July 12, 2021. Recall level: Level 3 Recall. Maikewei (Shanghai) Medical Equipment Co., Ltd. initiated a voluntary Class III recall for its dipol

---

## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Maco (Shanghai) Medical Equipment Co., Ltd. has initiated a voluntary recall of its bifid braided artificial blood vessels.
- Company Name: Maikewei (Shanghai) Medical Equipment Co., Ltd.
- Publication Date: 2021-07-12
- Product Name: Diffused braided artificial blood vessels
- Recall Level: Level 3 Recall
- Recall Reason: The specifications on the inner and outer packaging labels of the product are inconsistent.
- Discovering Company: Maikewei (Shanghai) Medical Equipment Co., Ltd.
- Manufacturing Company: Maikewei (Shanghai) Medical Equipment Co., Ltd.
- Summary: Maikewei (Shanghai) Medical Equipment Co., Ltd. initiated a voluntary Class III recall for its dipolluted braided artificial blood vessels. This action, reported to the National Medical Products Administration (NMPA) via the Shanghai Municipal Drug Administration on July 12, 2021, stems from a reported complaint concerning inconsistencies between the specifications displayed on the inner and outer packaging labels of the affected products. The company undertook this recall out of a commitment to patient safety and to ensure the continued safe use of its medical devices. While specific inspection dates are not provided in the document, the recall decision was made by the manufacturer upon receiving the complaint. The regulatory framework under which this recall proceeds is established by the NMPA, overseeing medical device safety. Maikewei (Shanghai) Medical Equipment Co., Ltd. is taking the required action of removing the affected products from the market to address the labeling discrepancies and uphold product integrity. Further details on specific models, specifications, and serial numbers are available in an attached Medical Device Recall Event Report Form.

Company: https://www.globalkeysolutions.net/companies/maikewei-shanghai-medical-equipment-co-ltd/77310e7c-a692-4918-a052-23f3348af2e9/