Device recall
Z-2325-2012: 100 ft roll of tubing inside a cardboard box. Medical devices are sealed into…
FDA device recall · Class III · Steris Corporation
Key facts
| Recall number (Z-number) | Z-2325-2012 |
|---|---|
| Recall event | 62852 |
| Product | 100 ft roll of tubing inside a cardboard box. Medical devices are sealed into the tubes prior to ethylene oxide sterilization. Tube maintains sterility of the enclosed medical devices until opened. |
| Product code | LRT |
| Recalling firm | Steris Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 4, 2013 |
| 510(k) numbers | K092745 |
| FEI number | 1527821 |
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