Device recall
Z-0865-2015: KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed…
FDA device recall · Class I · Halyard Health
Key facts
| Recall number (Z-number) | Z-0865-2015 |
|---|---|
| Recall event | 69910 |
| Product | KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 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. |
| Product code | BTR |
| Recalling firm | Halyard Health |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 18, 2015 |
| 510(k) numbers | K131254 |
| FEI number | 3011157493 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database