Device recall
Z-0975-2018: IMRIS ORT100 Table, Part Number 110470-000
FDA device recall · Class II · Deerfield Imaging, Inc.
Key facts
| Recall number (Z-number) | Z-0975-2018 |
|---|---|
| Recall event | 79360 |
| Product | IMRIS ORT100 Table, Part Number 110470-000 |
| Product code | KXJ |
| Recalling firm | Deerfield Imaging, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 27, 2019 |
| 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