Device recall
Z-2119-2008: 10mm Bone Graft Drill. Product labeled in part, "ACUMED 5885 NW Cornelius pass…
FDA device recall · Class II · Acumed LLC
Key facts
| Recall number (Z-number) | Z-2119-2008 |
|---|---|
| Recall event | 48453 |
| Product | 10mm Bone Graft Drill. Product labeled in part, "ACUMED 5885 NW Cornelius pass Road Hillsboro, OR. 97124-9432... Size: 10mm Bone Graft Drill... REF BG-8020-S ... LOT W54076". |
| Product code | HWC |
| Recalling firm | Acumed LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 3, 2010 |
| 510(k) numbers | K960711 |
| FEI number | 1000125930 |
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