Recall Radar · 美国食品召回雷达
FDA Recalls, Market Withdrawals & Safety Alerts · Other / 其他Trilogy Evo, Trilogy Evo O2, Trilogy Evo Universal, and Trilogy EV300 ventilators
Official-information notice / 官方信息说明: This page transcribes fields from the named agency record. It is not medical, legal, or food-safety advice. Follow the agency's original notice and instructions.
Recall number / 召回编号
fda-alert:2024-10-07:Philips Respironics:Trilogy Evo, Trilogy Evo O2, Trilogy Evo Universal, and Trilogy EV300 ventilators
Classification / 风险等级
Other / 其他
Published / 发布时间
2024-10-07
Recalling firm / 召回企业
Philips Respironics, Inc.
Product description / 产品描述
Trilogy Evo, Trilogy Evo O2, Trilogy Evo Universal, and Trilogy EV300 ventilators
Product code / 产品代码
Not provided in the official record
Code information / 批次与代码信息
Not provided in the official record
Product quantity / 产品数量
Not provided in the official record
Distribution / 销售地区
Not provided in the official record
Reason for recall / 召回原因
The use of in-line nebulizers placed in certain locations may lead to aerosol deposits forming over time on the ventilator flow sensor. Should this occur, there is a possibility of inaccurate flow measurements affecting therapy.
Open official source ↗ / 打开官方来源
Last synchronized: 2024-10-07. Recall Radar does not replace agency guidance.