Device recall
Z-2067-2009: Portex Tracheal Tube, Oral/Nasal, Murphy Eye, Siliconized, 3.5 mm Product Code…
FDA device recall · Class I · Smiths Medical
Key facts
| Recall number (Z-number) | Z-2067-2009 |
|---|---|
| Recall event | 53075 |
| Product | Portex Tracheal Tube, Oral/Nasal, Murphy Eye, Siliconized, 3.5 mm Product Code: 100/141/035. Intended for oral and/or nasal intubation for airway management. |
| Product code | BTR |
| Recalling firm | Smiths Medical |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 16, 2012 |
| FEI number | 3002807908 |
At a glance
- None Linked 510(k)s
- 10–99 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