Device recall
Z-2109-2008: 4 Hole Locking 1st Tarsometatarsal Plate. Product labeled in part, "ACUMED 5885…
FDA device recall · Class II · Acumed LLC
Key facts
| Recall number (Z-number) | Z-2109-2008 |
|---|---|
| Recall event | 48453 |
| Product | 4 Hole Locking 1st Tarsometatarsal Plate. Product labeled in part, "ACUMED 5885 NW Cornelius pass Road Hillsboro, OR. 97124-9432... Size: 4 Hole Locking 1st Tarsometatarsal Plate... REF 70-0008-S... LOT W58116". |
| Product code | HWC |
| Recalling firm | Acumed LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 3, 2010 |
| 510(k) numbers | K033639 |
| 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