Recall Radar · 美国食品召回雷达
FDA Recalls, Market Withdrawals & Safety Alerts · Other / 其他SubG Endotracheal Tubes with Subglottic Suction and kits that contain these devices
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:2024-05-31:Medline:SubG Endotracheal Tubes with Subglottic Suction and kits that contain these devices
Classification / 风险等级
Other / 其他
Published / 发布时间
2024-05-31
Recalling firm / 召回企业
Medline Industries LP
Product description / 产品描述
SubG Endotracheal Tubes with Subglottic Suction and kits that contain these devices
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 inflation tube and other device components have become detached and/or torn from the main tube, resulting in moisture buildup, loss of pressure, or inability to inflate.
Open official source ↗ / 打开官方来源
Last synchronized: 2024-05-31. Recall Radar does not replace agency guidance.