FDA Device recall Z-0868-2015
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 8.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway manage…
- FDA Device
- Class I
- terminated
- Published 2014-12-31
On 2014-12-31 the FDA classified a Class I recall of KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 8.5 mm, Distributed by Kimberly Clark Global Sales, LLC. Used for airway manage… by Halyard Health, citing the cuff inflation line may detach from the endotracheal tube during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0868-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-11-17 |
| Published | 2014-12-31 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Halyard Health |
| Distribution | US |
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.
Reason
The cuff inflation line may detach from the endotracheal tube during use.
Identifiers
| code_info | Product Code: 13223, Lot numbers: AA3203V03, AA3234, AA3234V01, AA3260, AA3260V01, AA4038, AA4038V01, AA4038V02, AA4038…Product Code: 13223, Lot numbers: AA3203V03, AA3234, AA3234V01, AA3260, AA3260V01, AA4038, AA4038V01, AA4038V02, AA4038V05, AA4077, AA4077V01, AA4083, AA4083V01, AA4092V01 & AA4125V02. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0868-2015%22
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