Device recall
Z-1315-2010: KODAK T-MAT G/RA Film, Catalog/REF # 151 0023, 24x30 cm, 5-100 Sheet Boxes…
FDA device recall · Class III · Carestream Health, Inc.
Key facts
| Recall number (Z-number) | Z-1315-2010 |
|---|---|
| Recall event | 54981 |
| Product | KODAK T-MAT G/RA Film, Catalog/REF # 151 0023, 24x30 cm, 5-100 Sheet Boxes FOLHAS/Hojas, Made in U.S.A. by Carestream Health, Inc. 150 Verona Street, Rochester, NY 14608 --- Device Listing # E420904 Intended use: Imaging film |
| Product code | IWZ |
| Recalling firm | Carestream Health, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 7, 2010 |
| 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