Device recall
Z-0155-2009: Allez Spine Cross Connectors; Catalog Number: LG-CC1001Cross Link, Small…
FDA device recall · Class II · Allez Spine, LLC
Key facts
| Recall number (Z-number) | Z-0155-2009 |
|---|---|
| Recall event | 49444 |
| Product | Allez Spine Cross Connectors; Catalog Number: LG-CC1001Cross Link, Small 30-37mm; LG-CC1002 Cross Link, Medium 37-50mm; LG-CC1003 Cross Link, Lange 50-80mm; lT-T01003 Cross Link Torque Hex Driver, 2.5mm |
| Product code | NKB |
| Recalling firm | Allez Spine, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 19, 2010 |
| 510(k) numbers | K070460 |
| FEI number | 3005032381 |
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