Device recall
Z-2153-2008: Acu-Loc Distal Radius Plate, Standard, Left. Product labeled in part, " Acu-Loc…
FDA device recall · Class III · Acumed LLC
Key facts
| Recall number (Z-number) | Z-2153-2008 |
|---|---|
| Recall event | 48466 |
| Product | Acu-Loc Distal Radius Plate, Standard, Left. Product labeled in part, " Acu-Loc Distal Radius Plate, Standard, Left... PL-DR50L W48003... Manufactured or Distributed by: Acumed LLC Hillsboro, OR ". |
| Product code | HRS |
| Recalling firm | Acumed LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 3, 2010 |
| 510(k) numbers | K012655 |
| FEI number | 1000125930 |
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