Device recall
Z-2236-2009: Action Products, Inc., Bol-X-II, 30x30x0.5cm, item number 32052, packaged…
FDA device recall · Class II · Action Products Incorporated
Key facts
| Recall number (Z-number) | Z-2236-2009 |
|---|---|
| Recall event | 53041 |
| Product | Action Products, Inc., Bol-X-II, 30x30x0.5cm, item number 32052, packaged 10/carton. Polymer pad used during radiation therapy. |
| Product code | JAD |
| Recalling firm | Action Products Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 29, 2009 |
| 510(k) numbers | K811528 |
| FEI number | 1181047 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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