Device recall
Z-0220-2007: Konica Minolta PrintLink III Model - ID/IV, code no. 0770, 0771 Medical Imaging…
FDA device recall · Class II · Konica Minolta Medical Imaging USA, Inc.
Key facts
| Recall number (Z-number) | Z-0220-2007 |
|---|---|
| Recall event | 36658 |
| Product | Konica Minolta PrintLink III Model - ID/IV, code no. 0770, 0771 Medical Imaging Communication Device Model IV - product code 5000230 Model ID, product code 5000330 Konica Minolta Medical & Graphic, Inc. No. 26-2, Nishishinjuku 1-chrome, Shinjuku-ku, Tokoyo 163-0512, Japan |
| Product code | LMD |
| Recalling firm | Konica Minolta Medical Imaging USA, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 1, 2008 |
| 510(k) numbers | K900227 |
| FEI number | 2241281 |
At a glance
- 1–9 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