Device recall
Z-2050-2009: Portex Continuous Epidural Tray, Reference 4037-20 An anesthesia conduction kit…
FDA device recall · Class III · Smiths Medical ASD, Inc.
Key facts
| Recall number (Z-number) | Z-2050-2009 |
|---|---|
| Recall event | 52695 |
| Product | Portex Continuous Epidural Tray, Reference 4037-20 An anesthesia conduction kit is a device used to administer to a patient conduction, regional, or local anesthesia. |
| Product code | BSO |
| Recalling firm | Smiths Medical ASD, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 14, 2012 |
| 510(k) numbers | K062005 |
| 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