Device recall
Z-0144-2015: IMRIS Operating Room table (ORT200 and ORT300). Intended for use during…
FDA device recall · Class II · IMRIS Inc
Key facts
| Recall number (Z-number) | Z-0144-2015 |
|---|---|
| Recall event | 69265 |
| Product | IMRIS Operating Room table (ORT200 and ORT300). Intended for use during diagnostic examinations or surgical procedures to support and position a patient. |
| Product code | FQO |
| Recalling firm | IMRIS Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 20, 2015 |
| FEI number | 3010326005 |
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