Device recall
Z-0571-2009: Stone Retrieval Basket Model #': BOS390-105 Used to entrap and remove renal…
FDA device recall · Class II · Sterilmed Inc
Key facts
| Recall number (Z-number) | Z-0571-2009 |
|---|---|
| Recall event | 49510 |
| Product | Stone Retrieval Basket Model #': BOS390-105 Used to entrap and remove renal stones and calculi via a rig id or flexible endoscope during transurethral or fluoroscopic percutaneous urologic procedures. |
| Product code | FFL |
| Recalling firm | Sterilmed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 26, 2011 |
| 510(k) numbers | K012581 |
| FEI number | 3001237663 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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