Device recall
Z-0996-03: Portex Uncuffed Oral/Nasal Tracheal Tube, Murphy Eye Clear 3.5 mm x 19cm…
FDA device recall · Class II · Portex Ltd.
Key facts
| Recall number (Z-number) | Z-0996-03 |
|---|---|
| Recall event | 26394 |
| Product | Portex Uncuffed Oral/Nasal Tracheal Tube, Murphy Eye Clear 3.5 mm x 19cm Reference Number: 100/127/035 |
| Recalling firm | Portex Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2006 |
| FEI number | 3002807908 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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