# China NMPA Product Recall - Medical compressor nebulizer

Source: https://www.globalkeysolutions.net/records/china_product_recall/dongguan-yinghua-rongtai-medical-technology-co-ltd/72d03d97-410f-49ad-bff0-67109c1fe80a/
Source feed: China

> China NMPA product recall for Medical compressor nebulizer by Dongguan Yinghua Rongtai Medical Technology Co., Ltd. published July 05, 2022. Recall level: Level 3 Recall. Dongguan Yinghua Rongtai Medical Technology Co., Ltd. has initiated a voluntary Class III recall of 

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## Details

- Record Type: CHINA_PRODUCT_RECALL
- Title: Dongguan Yinghua Rongtai Medical Technology Co., Ltd. voluntarily recalls medical compressor nebulizers
- Company Name: Dongguan Yinghua Rongtai Medical Technology Co., Ltd.
- Publication Date: 2022-07-05
- Product Name: Medical compressor nebulizer
- Recall Level: Level 3 Recall
- Recall Reason: Non-compliance with standards was discovered during routine management.
- Discovering Company: Dongguan Yinghua Rongtai Medical Technology Co., Ltd.
- Manufacturing Company: Dongguan Yinghua Rongtai Medical Technology Co., Ltd.
- Summary: Dongguan Yinghua Rongtai Medical Technology Co., Ltd. has initiated a voluntary Class III recall of its medical compressed nebulizers. The recall specifically targets model FA03, with batch number 220425. This action stems from the discovery of non-compliance with established standards during the company's routine internal management processes. Publicized by the National Medical Products Administration (NMPA) and originating from the Guangdong Provincial Drug Administration Website on July 5, 2022, this recall underscores the company's commitment to product safety and regulatory adherence. While the specific nature of the non-compliance is not detailed, it indicates a deviation from required quality or performance benchmarks for the medical device. Dongguan Yinghua Rongtai Medical Technology Co., Ltd. is undertaking necessary steps to remove the affected products from the market, with detailed information available in a "Medical Device Recall Event Report Form." This voluntary recall reflects a proactive approach within the NMPA's regulatory framework to address product deficiencies and ensure public health. The Class III classification suggests that the identified non-compliance is unlikely to cause adverse health consequences but still warrants corrective action.

Company: https://www.globalkeysolutions.net/companies/dongguan-yinghua-rongtai-medical-technology-co-ltd/5464129a-09cf-4925-9b48-f4b5e6dff409/