# China NMPA Product Recall - Heart-Lung Transfer Heat Exchanger Unit

Source: https://www.globalkeysolutions.net/records/china_product_recall/maquet-cardiopulmonary-ag/d511163b-929a-404f-b615-4a45bbbf53de/
Source feed: China

> China NMPA product recall for Heart-Lung Transfer Heat Exchanger Unit by MAQUET Cardiopulmonary AG published December 28, 2023. Recall level: Level 3 Recall. Maquet Cardiopulmonary GmbH, the manufacturer, has initiated a voluntary Class III recall for its He

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Maquet Cardiopulmonary GmbH is voluntarily recalling its cardiopulmonary bypass heat exchange tanks.
- Company Name: MAQUET Cardiopulmonary AG
- Publication Date: 2023-12-28
- Product Name: Heart-Lung Transfer Heat Exchanger Unit
- Recall Level: Level 3 Recall
- Recall Reason: The five HCU40 units in Slovakia, Bulgaria, Croatia, and Lithuania did not come with instruction manuals in their respective local languages.
- Discovering Company: Maikewei (Shanghai) Medical Equipment Co., Ltd.
- Manufacturing Company: MAQUET Cardiopulmonary AG
- Summary: Maquet Cardiopulmonary GmbH, the manufacturer, has initiated a voluntary Class III recall for its Heart-Lung Borough Heat-Cooler Units. This action was formally reported by Maquet (Shanghai) Medical Equipment Co., Ltd., and publicly announced by the National Medical Products Administration (NMPA). The recall specifically targets five HCU40 units that were distributed in Slovakia, Bulgaria, Croatia, and Lithuania. The core issue identified leading to this recall is the failure to provide instruction manuals in the local languages of the respective countries where the medical devices were distributed. This omission is a significant compliance concern, as accessible and comprehensible instructions are paramount for the safe and effective operation of medical equipment by healthcare professionals. Such documentation is vital for understanding proper usage, maintenance, and potential risks, directly impacting patient safety and device efficacy. Operating under the regulatory framework of the NMPA, these Heart-Lung Borough Heat-Cooler Units are recognized through National Medical Device Registration Certificate No. 20182451979. The Class III designation for this recall typically signifies that the product defect is unlikely to cause adverse health consequences, but the non-compliance still warrants corrective action. Although specific inspection dates are not mentioned, the voluntary recall demonstrates the company's commitment to addressing regulatory discrepancies. The required action for Maquet Cardiopulmonary GmbH involves managing the recall process efficiently. Comprehensive details regarding the specific products affected, including pricing and batch numbers, are documented in the "Medical Device Recall Event Report Form" provided by Maikewei (Shanghai) Medical Equipment Co., Ltd., ensuring full transparency and enabling swift action by distributors and users. This measure aims to rectify the instructional deficiency and uphold regulatory standards across international markets.

Company: https://www.globalkeysolutions.net/companies/maquet-cardiopulmonary-ag/63ce4d48-8350-4a6e-bbe2-5003aa14ae22/