China NMPA Product Recall - Disposable medical masks
Discuss this record with AI
Anhui Yimeijian Medical Supplies Co., Ltd. initiated a voluntary Class III recall for a specific batch of its disposable medical masks, identified by batch number 20201208. This action, reported by the National Medical Products Administration (NMPA) on May 26, 2022, stems from a failure to meet quality standards during a random inspection. The main issue was the product's non-compliance with established quality parameters, rendering it unsuitable for its intended medical use. Under the regulatory oversight of the NMPA, which governs medical device safety and efficacy, the company is required to remove the violative product from circulation. A Class III recall typically signifies that while a product violates regulations, its use is unlikely to cause severe adverse health consequences. Comprehensive details regarding the affected models, specifications, and batch numbers are available in the accompanying "Medical Device Recall Event Report Form." This proactive measure aims to uphold product safety and public health by ensuring non-compliant devices are effectively withdrawn from the market.
ID · 2a9d2342-8b1a-4d3f-aa73-cd21270e65aa