Device recall
Z-1641-2014: Portex Low Dead Space Connector with Sideport, 3.5mm Product Usage: The…
FDA device recall · Class I · Smiths Medical ASD, Inc.
Key facts
| Recall number (Z-number) | Z-1641-2014 |
|---|---|
| Recall event | 67991 |
| Product | Portex Low Dead Space Connector with Sideport, 3.5mm Product Usage: The connector is used to attach the endotracheal tube to the patient breathing circuit. The low dead space connector minimizes mechanical dead space and subsequent carbon dioxide rebreathing. The connector's sideport permits access… |
| Product code | BTR |
| Recalling firm | Smiths Medical ASD, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 29, 2016 |
| 510(k) numbers | K790312 |
| FEI number | 1217052 |
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