Device recall
Z-0129-2007: Sheridan T.T.X. Tracheal Tube Exchanger, Large Size for tracheal tube sizes 7.5…
FDA device recall · Class III · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0129-2007 |
|---|---|
| Recall event | 36426 |
| Product | Sheridan T.T.X. Tracheal Tube Exchanger, Large Size for tracheal tube sizes 7.5 mm - 10.0 mm; a Rx, sterile, single use tracheal tube exchanger; Hudson Respiratory Care Inc., Temecula, CA 92589-9020, Manufactured in Mexico; catalog number (REF) 5-24006 |
| Product code | LNZ |
| Recalling firm | Teleflex Medical |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 12, 2009 |
| 510(k) numbers | K862347 |
| FEI number | 3004959265 |
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