Device recall
Z-0999-03: Portex Profile Soft-Seal Cuff Oral/Nasal Tracheal Tube, Clear Murphy Eye 8 mm x…
FDA device recall · Class II · Portex Ltd.
Key facts
| Recall number (Z-number) | Z-0999-03 |
|---|---|
| Recall event | 26394 |
| Product | Portex Profile Soft-Seal Cuff Oral/Nasal Tracheal Tube, Clear Murphy Eye 8 mm x 33cm Reference Number: 100/199/080 |
| 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