China NMPA Product Recall - Soft contact lenses

Johnson & Johnson Vision Care Trading (Shanghai) Co., Ltd. initiated a voluntary recall of specific soft contact lenses on December 7, 2017, as reported by the National Medical Products Administration (NMPA). The recall was prompted by the discovery of visible foreign objects located between the plastic case and aluminum foil packaging of the affected products. The recalled items include soft contact lenses with registration numbers (Imported) 2012 No. 3221445, CFDA (Imported) 2014 No. 3224691, and CFDA (Imported) 2014 No. 3224684, marketed under trade names such as BrightEye and Oculus. This action falls under the NMPA's regulatory oversight for medical devices, ensuring product safety and quality within the market. As part of the recall process, Johnson & Johnson Vision Care Trading (Shanghai) Co., Ltd. is required to provide comprehensive details regarding the recall level, specific product models, specifications, and batch numbers. This information is outlined in an accompanying "Medical Device Recall Event Report Form" to facilitate the efficient retrieval and management of the affected lenses. The voluntary recall demonstrates the company's commitment to addressing product deficiencies and complying with regulatory standards to protect consumer health.