Device recall
Z-1515-2008: SEQUENCER, MOSAIQ versions 1.3 and 1.4 with Elekta and Siemens Machines, Model…
FDA device recall · Class II · Impac Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-1515-2008 |
|---|---|
| Recall event | 46941 |
| Product | SEQUENCER, MOSAIQ versions 1.3 and 1.4 with Elekta and Siemens Machines, Model number 40003-001000-RO, Manufactured by IMPAC Medical Systems, Sunnyvale, CA. Used to facilitate the delivery of defined radiotherapy treatment plans. |
| Product code | IYE |
| Recalling firm | Impac Medical Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 24, 2009 |
| 510(k) numbers | K981313 |
| FEI number | 1000123805 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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