Device recall
Z-0817-05: KODAK GP FLEXIBLE PHOSPHOR SCREENS, for use with Kodak DirectView CR 500…
FDA device recall · Class II · Eastman Kodak Co
Key facts
| Recall number (Z-number) | Z-0817-05 |
|---|---|
| Recall event | 31494 |
| Product | KODAK GP FLEXIBLE PHOSPHOR SCREENS, for use with Kodak DirectView CR 500 systems. Responsible firm on label: Made in U.S.A. by Eastman Kodak Company, Rochester, N.Y. 14650. Screens are sold in the following sizes and Cat. Nos: (1) Cat. #812-7334 - 15 x 30 cm; (2) Cat #825-9269 - 18 x 24 cm; (3) Cat… |
| Product code | IXJ |
| Recalling firm | Eastman Kodak Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 19, 2005 |
| 510(k) numbers | K925997 |
| FEI number | 1315356 |
At a glance
- 1–9 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