China NMPA Product Recall - Portable ultrasonic nebulizer

On January 6, 2022, the National Medical Products Administration (NMPA) announced a voluntary recall initiated by Shenzhen Raffles Nebulizer Medical Co., Ltd. The recall targets specific portable ultrasonic nebulizers from production batch number 20180522004. This action followed a random inspection which identified that products within this batch did not meet established quality standards. While explicit inspection dates were not detailed, the findings prompted Shenzhen Raffles Nebulizer Medical Co., Ltd. to proactively recall the non-compliant medical devices. This event underscores the NMPA’s role in overseeing medical product safety and market compliance. The company’s voluntary recall reflects its commitment to patient safety and adherence to regulatory requirements for medical devices. Further comprehensive details, including affected models and specifications, are available in the "Medical Device Recall Event Report Form" to guide consumers and healthcare professionals on necessary actions regarding the recalled products.