Device recall
Z-1178-06: Theratron 780C Cobalt Radiotherapy
FDA device recall · Class II · MDS Canada Inc. DBA MDS Nordion
Key facts
| Recall number (Z-number) | Z-1178-06 |
|---|---|
| Recall event | 35617 |
| Product | Theratron 780C Cobalt Radiotherapy |
| Product code | IWB |
| Recalling firm | MDS Canada Inc. DBA MDS Nordion |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 27, 2006 |
| 510(k) numbers | K001006 |
| FEI number | 3001092088 |
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