Smiths Medical ASD today announced the Class I recall of its PneuPac paraPAC Plus 300 and 310 ventilator kits after receiving complaints reporting continuous positive gas flow instead of the intended ...
Smiths Medical is recalling its paraPAC Plus ventilators because of the possibility that the patient outlet connector could loosen or detach, affecting active ventilation. The FDA labeled the recall ...
史密斯集团（“史密斯”）在其位于英国卢顿的史密斯医疗设施中大幅增加了其PARAPAC Plus呼吸机的产量。 史密斯作为英国联盟的核心成员，致力于通过提供PARAPAC Plus设备来实现英国政府制定的3 ...
近日，FDA官网发布消息称，其正在升级 Smiths Medical的三套呼吸硬件召回，包括通过颈部进入气道的便携式呼吸机和气管切开插管。FDA将每款产品都归类为I级召回，这是其最严重的类型。 据悉 ...
来源：器械之家，未经授权不得转载，且24小时后方可转载。 4月4日，在收到8起与严重伤害有关的故障报告后，美国FDA宣布将Smiths Medical旗下的Pneupac Parapac Plus 300和310呼吸机套件召回定为一级 ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results