Device recall
Z-1391-05: Regius-IM. The Regius Image Manager for Centralized workflow and improved image…
FDA device recall · Class III · Konica Medical Imaging, Inc.
Key facts
| Recall number (Z-number) | Z-1391-05 |
|---|---|
| Recall event | 32068 |
| Product | Regius-IM. The Regius Image Manager for Centralized workflow and improved image quality software. |
| Product code | LMA |
| Recalling firm | Konica Medical Imaging, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 31, 2005 |
| FEI number | 2241281 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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