Device recall
Z-0166-04: Portex Spinal Tray with 25G Whitacre Needle. Kit contains Bupivacaine in…
FDA device recall · Class II · Portex Inc
Key facts
| Recall number (Z-number) | Z-0166-04 |
|---|---|
| Recall event | 27470 |
| Product | Portex Spinal Tray with 25G Whitacre Needle. Kit contains Bupivacaine in Dextrose, Epinephrine,Lidocaine, Lidocaine in Dextrose and Tetracaine Catalog Number: 15545-20 |
| Product code | CAZ |
| Recalling firm | Portex Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 2, 2006 |
| 510(k) numbers | K965017 |
| 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