Device recall
Z-0830-03: C1140 Flexible Endoscope Processing Container and Tray assembly.
FDA device recall · Class II · Steris Corp
Key facts
| Recall number (Z-number) | Z-0830-03 |
|---|---|
| Recall event | 26151 |
| Product | C1140 Flexible Endoscope Processing Container and Tray assembly. |
| Product code | MLR |
| Recalling firm | Steris Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2004 |
| 510(k) numbers | K875280 |
| FEI number | 1527821 |
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