U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
데이터 추가 비고
Needle, Fistula - Product Code FIE
원인
Air or fluid leakage at the hub/needle junction.
조치
The recall letters were mailed on November 8, 2002 to direct accounts and requested subrecall down to the health professional/clinic level. It was requested that Nipro be notified of all held and recovered product for pickup. Also new replacement product will be made available in the near future.
The following brand name labeled products are under recall (all || catalog numbers and all lot numbers under recall): || NIPRO SafeTouch Safety Fistula Needle, Baxter Safety AV Fistula || Set and EXEL Secure Touch Safety AV Fistula Needle Set.