Device recall
Z-0052-2012: Impac Medical Systems Sequencer Product Usage: The intended us of Sequencer is…
FDA device recall · Class II · Impac Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-0052-2012 |
|---|---|
| Recall event | 59961 |
| Product | Impac Medical Systems Sequencer Product Usage: The intended us of Sequencer is to assists in the process of patient treatment on a radiotherapy treatment machine. Sequencer provides the capability to notify the user of actions that need to take place prior to treatment, to display reference images… |
| Product code | IYE |
| Recalling firm | Impac Medical Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 6, 2012 |
| 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