China NMPA Product Recall - Disposable suction catheter

Nantong Sanli Medical Device Co., Ltd. initiated a voluntary Class III recall of its disposable suction catheters, as announced on February 25, 2019, under the oversight of the National Medical Products Administration (NMPA). The recall was prompted by critical product defects, including deformation of the catheter tip and other manufacturing issues affecting the suction catheters. This proactive measure addresses quality control deficiencies and potential safety concerns. Although specific inspection dates were not provided in the document, the company's action demonstrates a commitment to resolving product non-conformities. The required action involves retrieving the affected products from the market. Comprehensive details regarding the specific models, specifications, and batch numbers of the recalled devices are documented in a separate 'Medical Device Recall Event Report Form' for reference.