# China NMPA Product Recall - Single-use lancet (finger lancet)

Source: https://www.keypedia.com/records/china_product_recall/xiamen-minsheng-medical-technology-co-ltd/4dc0de56-18a0-4e40-860d-e7af6fdabbcb
Source feed: China

> China NMPA product recall for Single-use lancet (finger lancet) by Xiamen Minsheng Medical Technology Co., Ltd. published March 30, 2022. Recall level: Level 3 Recall. Xiamen Minsheng Medical Technology Co., Ltd. has voluntarily initiated a Class III recall for a spec

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Xiamen Minsheng Medical Technology Co., Ltd. is voluntarily recalling single-use lancets (for fingers).
- Company Name: Xiamen Minsheng Medical Technology Co., Ltd.
- Publication Date: 2022-03-30
- Product Name: Single-use lancet (finger lancet)
- Recall Level: Level 3 Recall
- Recall Reason: The registration certificate number on the outer packaging box of a single-use finger lancet (batch number: 20210601) is printed incorrectly. The registration certificate number on the outer packaging box should read "闽械注准20152220157" instead of "闽械注准20152410157".
- Discovering Company: Xiamen Minsheng Medical Technology Co., Ltd.
- Manufacturing Company: Xiamen Minsheng Medical Technology Co., Ltd.
- Summary: Xiamen Minsheng Medical Technology Co., Ltd. has voluntarily initiated a Class III recall for a specific batch (20210601) of its single-use finger lottery needles. This action was prompted by a printing error on the outer packaging, where the product's registration certificate number was incorrectly displayed. The correct registration certificate numbers, as originally approved, are “闽械注准20152220157” and “闽械注准20152410157”. This recall falls under the regulatory framework of the National Medical Products Administration (NMPA) of China, with the announcement made public via the Fujian Provincial Drug Administration website. A Class III recall typically indicates that the product defect, while a deviation from regulatory requirements, is unlikely to cause serious adverse health consequences. As a required action, Xiamen Minsheng Medical Technology Co., Ltd. is actively retrieving all affected products from the market. The company has prepared a detailed "Medical Device Recall Event Report" that provides comprehensive information on the specific product models, specifications, and quantities involved in this recall. This measure underscores the company's commitment to maintaining accuracy in product labeling and adherence to the stringent regulatory standards set forth by the NMPA.

Company: https://www.keypedia.com/companies/xiamen-minsheng-medical-technology-co-ltd/3f1c0fae-cad2-4b57-a351-5b86e06308f6