Food and Drug Administration: Smith recalls more than 45,000 fluid containers

Medical Network March 14th According to the news from the State Food and Drug Administration website on the 13th, Smith Medical Devices Co., Ltd. voluntarily recalled 45,072 liquid reservoirs.

Smith medical instruments (Beijing) Co., Ltd. reported that due to the company proxy Some of the CADD fluid cartridges without run-off protection use the wrong pressure plate during the manufacturing process, which may result in partial or complete occlusion of the infusion tube, resulting in insufficient medication for the patient. Manufacturer Smiths Medical ASD, Inc. Liquid Box (Registration Certificate No.: National Food and Drug Administration <进>Word 2014 No. 3543474) Voluntary recall. The recall level is one level.