Device recall
Z-2426-2012: STERIS 5085 and 5085 SRT Surgical Tables, Product Usage: The 5085 is a general…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-2426-2012 |
|---|---|
| Recall event | 63142 |
| Product | STERIS 5085 and 5085 SRT Surgical Tables, Product Usage: The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal table top elevation. It accommodates all general surgical procedures including but not limited to, cardiac and vascular… |
| Product code | GDC |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 4, 2013 |
| 510(k) numbers | K090136 |
| 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