I heard that a patient suffered anaphylactic shock while using the Aier hemoperfusion device, and was stopped by the Food and Drug Administration? Who knows the specific situation?

Adverse reactions of Aier’s hemoperfusion device were stopped (reprinted)

Author: wjyk09 Submission date: 2009-8-9 16:45:00 Visits: 8 Replies: 0 Today Liuzhou News (Reporter Chen Xiaoyan) The reporter learned from the Liuzhou Food and Drug Administration yesterday that after days of inspections, the city has not found any "disposable hemoperfusion devices" that the district Food and Drug Administration requested to immediately suspend the sale and use.

It is understood that according to the report of the Autonomous Region Adverse Drug Reaction Monitoring Center, as of July 17, 3 hospitals in Guangxi are using products labeled as "disposable blood purification equipment produced by Langfang Aier Blood Purification Equipment Factory" "Infusion Device" (involving batch numbers: 20090430, 20090417, 20090601, 20090325), 11 cases of adverse events occurred, including 8 cases of anaphylactic shock, 1 case of skin itching, and 2 cases of chest tightness and local numbness.

In order to ensure the safety of public equipment and prevent the further expansion of adverse events, the Food and Drug Administration of the Autonomous Region has decided to suspend the sale and use of disposable hemoperfusion devices labeled with the above manufacturers and batch numbers throughout the region. .

After receiving the notice on the 18th, the Liuzhou Food and Drug Administration issued an emergency inspection notice to medical institutions and medical device business units in the city. As of 6 pm yesterday, according to feedback from some units, the above-mentioned products have not been found in Liuzhou City. At present, the inventory work is still in progress.

Quoted from: /gstg-20090718-1.htm Today's Liuzhou News (Reporter Chen Xiaoyan) The reporter learned from the Liuzhou Food and Drug Supervision Bureau yesterday that after days of inspections, the city has not found any food and drug supervision cases. The Bureau requires an immediate suspension of the sale and use of "single-use hemoperfusion devices".