Device recall
Z-2243-2016: Parker Trach-Vac Endotracheal Tubes. Tyvek pouches, 10 per box. Product Usage…
FDA device recall · Class II · Parker Medical
Key facts
| Recall number (Z-number) | Z-2243-2016 |
|---|---|
| Recall event | 74547 |
| Product | Parker Trach-Vac Endotracheal Tubes. Tyvek pouches, 10 per box. Product Usage: The product is an endotracheal tube with sub-glottic suction channel to remove secretions. It is used for intubating patients and used with a ventilator to provide oxygen or anesthetic agents to the patient. |
| Product code | BTR |
| Recalling firm | Parker Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 31, 2017 |
| 510(k) numbers | K110269 |
| FEI number | 3002986772 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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