Halyard Health KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 8.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space. Recall
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 8.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway management by oral intubation of the trachea and for removal of secretions that accumulate in the subglottic space.
Brand
Halyard Health
Lot Codes / Batch Numbers
Product Code: 13223, Lot numbers: AA3203V03, AA3234, AA3234V01, AA3260, AA3260V01, AA4038, AA4038V01, AA4038V02, AA4038V05, AA4077, AA4077V01, AA4083, AA4083V01, AA4092V01 & AA4125V02.
Products Sold
Product Code: 13223, Lot numbers: AA3203V03, AA3234, AA3234V01, AA3260, AA3260V01, AA4038, AA4038V01, AA4038V02, AA4038V05, AA4077, AA4077V01, AA4083, AA4083V01, AA4092V01 & AA4125V02.
Halyard Health is recalling KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 8.5 mm, Distributed by Kimberly Clark Gl due to The cuff inflation line may detach from the endotracheal tube during use.. This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The cuff inflation line may detach from the endotracheal tube during use.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026