Device recall
Z-2532-2026: Acumed Hexalob Screw various sizes: REF Numbers:: 3070-27008 2.7mm x 8mm NL…
FDA device recall · Class II · Acumed LLC
Key facts
| Recall number (Z-number) | Z-2532-2026 |
|---|---|
| Recall event | 99123 |
| Product | Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL Hexalobe Screw; 3070-27010 2.7mm x 10mm NL Hexalobe Screw; 3070-27011 2.7mm x 11mm NL Hexalobe Screw; 3070-27012 2.7mm x 12mm NL Hexalobe Screw; 3070-27013 2.7mm x 13mm NL Hexalobe… |
| Product code | HRS |
| Recalling firm | Acumed LLC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K251132, K251296 |
| 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