# China NMPA Product Recall - Ventilator

Source: https://www.globalkeysolutions.net/records/china_product_recall/weinmann-emergency-medical-technology-gmbh-cokg/e0231ffe-499b-42c7-9dc1-cfe00038273f/
Source feed: China

> China NMPA product recall for Ventilator by WEINMANN Emergency Medical Technology GmbH + Co.KG published January 13, 2025. Recall level: . The National Medical Products Administration (NMPA) issued an alert on January 13, 2025, announcing 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: WEINMANN Emergency Medical Technology GmbH + Co.KG initiates voluntary recall of ventilators.
- Company Name: WEINMANN Emergency Medical Technology GmbH + Co.KG
- Publication Date: 2025-01-13
- Product Name: Ventilator
- Recall Reason: The device may misinterpret high-frequency airflow as "pseudo-breathing," thus affecting the accuracy of etCO2 measurements.
- Discovering Company: Viman (Shanghai) Medical Device Trading Co., Ltd.
- Manufacturing Company: WEINMANN Emergency Medical Technology GmbH + Co.KG
- Summary: The National Medical Products Administration (NMPA) issued an alert on January 13, 2025, announcing a voluntary recall initiated by WEINMANN Emergency Medical Technology GmbH + Co.KG. Reported by WEINMANN (Shanghai) Medical Device Trading Co., Ltd., this recall pertains to specific Ventilators, identified by National Medical Device Registration Certificate 20153081989. The core issue driving this action is a functional anomaly where the device may inaccurately interpret high-frequency airflow as "false breathing." This technical deficiency significantly compromises the precision of etCO2 measurements, a critical parameter for effective patient ventilation and monitoring. 

The manufacturer's decision to undertake this voluntary recall underscores its commitment to maintaining product safety and performance standards. This action is conducted under the regulatory framework of the NMPA, the authoritative body for medical device oversight in China, ensuring public health and safety. While specific inspection dates were not provided, the recall date marks the public notification of this critical issue. The required action involves the immediate recall of affected Ventilators from the market. Comprehensive details, including specific models, technical specifications, and batch numbers of the products involved, are documented in the "Medical Device Recall Event Report Form" referenced in the official notice. It is confirmed that the products subject to this recall are domestic and not imported.

Company: https://www.globalkeysolutions.net/companies/weinmann-emergency-medical-technology-gmbh-cokg/2f143c2c-6365-4856-8bdd-ba14924824da/