Device recall
Z-1481-06: Regius Model 370 Digital Radiography Konica Minolta
FDA device recall · Class III · Konica Minolta Medical Imaging USA, Inc.
Key facts
| Recall number (Z-number) | Z-1481-06 |
|---|---|
| Recall event | 36109 |
| Product | Regius Model 370 Digital Radiography Konica Minolta |
| Product code | MQB |
| Recalling firm | Konica Minolta Medical Imaging USA, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 5, 2006 |
| 510(k) numbers | K051418 |
| FEI number | 2241281 |
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