# China NMPA Product Recall - Multifunctional incubator

Source: https://www.globalkeysolutions.net/records/china_product_recall/general-medical-equipment-shanghai-co-ltd/d0d0ce72-4230-4c4f-b093-898893da4cca
Source feed: China

> China NMPA product recall for Multifunctional incubator by General Medical Equipment (Shanghai) Co., Ltd. published August 03, 2020. Recall level: Level 3 Recall. On August 3, 2020, Dräger Medical Equipment (Shanghai) Co., Ltd. initiated a voluntary Class III rec

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Dräger Medical Equipment (Shanghai) Co., Ltd. is voluntarily recalling its multi-functional incubator.
- Company Name: General Medical Equipment (Shanghai) Co., Ltd.
- Publication Date: 2020-08-03
- Product Name: Multifunctional incubator
- Recall Level: Level 3 Recall
- Recall Reason: The product name on the cover of the instruction manual (version 9055056-04) for the Babyleo TN500 multi-functional incubator is "Infant Incubator," which is inconsistent with the product name "Multi-functional Incubator" in the approved registration certificate.
- Discovering Company: Dräger Medical Equipment (Shanghai) Co., Ltd.
- Manufacturing Company: General Medical Equipment (Shanghai) Co., Ltd.
- Summary: On August 3, 2020, Dräger Medical Equipment (Shanghai) Co., Ltd. initiated a voluntary Class III recall for its Babyleo TN500 multifunctional incubators, specifically version 9055056-04. This action was prompted by a significant inconsistency identified in the product labeling. The primary issue was that the product name displayed on the incubator's cover, "Infant Incubator," did not match the officially approved product name, "Multifunctional Incubator," as stated in its registration certificate (No.: 国械注进20183540187).

This recall, overseen by the National Medical Products Administration (NMPA) and the Shanghai Municipal Drug Administration, highlights the importance of precise labeling and adherence to regulatory documentation for medical devices. A Class III recall typically signifies a situation where the use of or exposure to a violative product is not likely to cause adverse health consequences. Dräger Medical Equipment (Shanghai) Co., Ltd. proactively reported this discrepancy, leading to the voluntary recall to ensure compliance and maintain product integrity. Detailed information regarding specific models, specifications, and batch numbers involved was provided in an attached Medical Device Recall Event Report Form. The company's immediate action underscores its commitment to regulatory standards and patient safety within the framework set by Chinese medical device regulations.

Company: https://www.globalkeysolutions.net/companies/general-medical-equipment-shanghai-co-ltd/e78bec1e-b5e6-44db-9c62-8b77dec44ed4