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.
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FDA Device · Class II · 2018-04-25 · Halyard Health - Halyard Closed Suction System for Adults, Turbo- cleaning¿Closed¿Suction¿System¿for¿Adults,¿Double¿Swivel¿Elbow (DSE). Used to aspirate liq…
FDA Device · Class II · 2018-04-25 · Halyard Health - CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with Electromagnetic Transmitting Stylet and CORFLO* Enteral Feeding tube, ANTI…
FDA Device · Class II · 2018-04-11 · Halyard Health - NOVAPLUS* Endotracheal WET PAK* Closed Suction System for Adults with BALLARD* Technology, Double Swivel Elbow, 14 F. 6 vials per kit, 20 k…
FDA Device · Class II · 2017-11-29 · Halyard Health
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0868-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.