Device recall
Z-0746-2012: DVB KODAK DRYVIEW --- 35x43 cm --- 125 SHT --- REF 8723132 --- Made in U.S.A. by…
FDA device recall · Class III · Carestream Health, Inc.
Key facts
| Recall number (Z-number) | Z-0746-2012 |
|---|---|
| Recall event | 60736 |
| Product | DVB KODAK DRYVIEW --- 35x43 cm --- 125 SHT --- REF 8723132 --- Made in U.S.A. by Carestream Health, Inc., 150 Verona St, Rochester, New York 14608. General purpose radiography. |
| Product code | IWZ |
| Recalling firm | Carestream Health, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 17, 2016 |
| FEI number | 1315356 |
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