Device recall
Z-1312-04: Shiley TracheoSoft XLT Extended Length Tracheostomy tube; Model Numbers…
FDA device recall · Class I · Nellcor Puritan Bennett
Key facts
| Recall number (Z-number) | Z-1312-04 |
|---|---|
| Recall event | 29653 |
| Product | Shiley TracheoSoft XLT Extended Length Tracheostomy tube; Model Numbers: 72110-050, size 5, Proximal Extension, Uncuffed; 72110-060, size 6, Proximal Extension, Uncuffed; 72110-070, size 7, Proximal Extension, Uncuffed; 72110-080, size 8, Proximal Extension, Uncuffed; 72120-050, size 5, Promixal… |
| Product code | --- |
| Recalling firm | Nellcor Puritan Bennett |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 29, 2005 |
| 510(k) numbers | K003315 |
| FEI number | 2936999 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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