Device recall
Z-1218-2024: Acu-Loc and Acu-Loc 2 bone plates, screws and accessories for the following REF…
FDA device recall · Class II · Acumed LLC
Key facts
| Recall number (Z-number) | Z-1218-2024 |
|---|---|
| Recall event | 93878 |
| Product | Acu-Loc and Acu-Loc 2 bone plates, screws and accessories for the following REF: 70-0045 Acu-Loc VDU Plate Standard, Left; 70-0045-S Acu-Loc VDU Plate Standard, Left; 70-0046 Acu-Loc VDU Plate Standard, Right; 70-0046-S Acu-Loc VDU Plate Standard, Right; 70-0047 Acu-Loc VDU Plate Long, Left… |
| Product code | HRS |
| Recalling firm | Acumed LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000125930 |
At a glance
- None 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