RESOLUTION OF EQUIPMENT SAFETY INCIDENTS & MANUFACTURES' RECALLS

卫生保健组织认证联合委员会 要求临床中心制定评估设备的计划 故障和用户错误。该方案的主要特点是： 1.调查涉及设备和病人或来访者的事故 或雇员。 2.处理设备制造商发出的召回通知，安全 组织和政府机构。 3.制定行动计划，以解决与以下方面有关的安全隐患： 设备. 4.参与解决安全隐患。 5.参与评估所采取行动的有效性。 为了完成这个项目，我们采访了病人、医务人员和支持人员。 以及其他涉及临床和非临床事件的人员 设备.我们与安全专员、临床中心和 安全处制定并执行纠正程序。 这通常涉及拆除设备， 制造商和临床工作人员的培训。我们还参加了 通过我们对医院的活动评估纠正措施 委员会。

The Joint Commission on Accreditation of Health Care Organizations requires the Clinical Center to have a program to evaluate equipment failures and user errors. The principal features of this program are: 1. Investigation of incidents involving equipment and patients or visitors or employees. 2. Processing of recall notices sent by equipment manufacturers, safety organizations and government agencies. 3. Formulation of a plan of action to resolve safety hazards related to equipment. 4. Participation in the resolution of the safety hazards. 5. Participation in the evaluation of effectiveness of actions taken. To accomplish the program we interview patients, medical and support staff and others involved in incidents involving clinical and nonclinical equipment. We work closely with the Safety Officer, Clinical Center and the Division of Safety to formulate and carry out corrective procedures. This often involves removal of equipment, modification of equipment by manufacturers and training of clinical staff. We also participate in the evaluation of corrective actions through our activity on hospital committees.