Device recall
Z-1717-2009: M-19 (Iridium 192): Source Production and Equipment Company, St. Rose, LA…
FDA device recall · Class II · Source Production & Equipment Inc
Key facts
| Recall number (Z-number) | Z-1717-2009 |
|---|---|
| Recall event | 52428 |
| Product | M-19 (Iridium 192): Source Production and Equipment Company, St. Rose, LA. Brachytherapy source. |
| Product code | KXK |
| Recalling firm | Source Production & Equipment Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 19, 2009 |
| 510(k) numbers | K052947 |
| FEI number | 1000437833 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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