Device recall
Z-0582-04: EPROM and Control Software (embedded), version 5.08, for the GammaMed 12i/t…
FDA device recall · Class II · Varian Medical Systems
Key facts
| Recall number (Z-number) | Z-0582-04 |
|---|---|
| Recall event | 28300 |
| Product | EPROM and Control Software (embedded), version 5.08, for the GammaMed 12i/t Afterloader, manufactured by Varian Medical Systems, Inc, Palo Alto, CA 94304. |
| Product code | JAQ |
| Recalling firm | Varian Medical Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 21, 2004 |
| FEI number | 3000206172 |
At a glance
- None 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