Device recall
Z-0952-03: Exradin A12 Ionization Chamber
FDA device recall · Class III · Standard Imaging Inc.
Key facts
| Recall number (Z-number) | Z-0952-03 |
|---|---|
| Recall event | 26445 |
| Product | Exradin A12 Ionization Chamber |
| Product code | IYE |
| Recalling firm | Standard Imaging Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 2, 2004 |
| FEI number | 1000115748 |
At a glance
- None 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