Device recall
Z-1417-2013: Copperhead IBFD, Large Neutral, 6mm Copperhead IBFD, Large Neutral, 7mm…
FDA device recall · Class II · Spinal Solutions, LLC
Key facts
| Recall number (Z-number) | Z-1417-2013 |
|---|---|
| Recall event | 64586 |
| Product | Copperhead IBFD, Large Neutral, 6mm Copperhead IBFD, Large Neutral, 7mm Copperhead IBFD, Large Neutral, 8mm Copperhead IBFD, Large Neutral, 9mm Copperhead IBFD, Large Neutral, 10mm Copperhead IBFD, Large Neutral, 11mm Product Usage: Spinal Solutions distributes a variety of spinal fixation devices… |
| Product code | MAX |
| Recalling firm | Spinal Solutions, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 26, 2014 |
| 510(k) numbers | K090064 |
| FEI number | 3004884943 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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