Device recall
Z-0885-05: Clinical Technologies, Inc., 25 G Spinal Painpak, Reorder No.:4043, kit…
FDA device recall · Class II · Spinal Specialties, Inc
Key facts
| Recall number (Z-number) | Z-0885-05 |
|---|---|
| Recall event | 31950 |
| Product | Clinical Technologies, Inc., 25 G Spinal Painpak, Reorder No.:4043, kit manufactured by Integra Spinal Specialties, San Antonio, Texas. |
| Product code | CAZ |
| Recalling firm | Spinal Specialties, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 2, 2005 |
| FEI number | 1000306134 |
At a glance
- None 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