Device recall
Z-1022-2010: SmartBlock Pain Management System, Part numbers P49524, P49534, P49624, and…
FDA device recall · Class II · Hsmg, Inc. D/b/a Smartinfuser Usa
Key facts
| Recall number (Z-number) | Z-1022-2010 |
|---|---|
| Recall event | 54089 |
| Product | SmartBlock Pain Management System, Part numbers P49524, P49534, P49624, and P49634. |
| Product code | MEB |
| Recalling firm | Hsmg, Inc. D/b/a Smartinfuser Usa |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 25, 2011 |
| 510(k) numbers | K072053 |
| FEI number | 3004960040 |
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