Device recall
Z-0554-2007: Cmax Surgical Table, Model No. 2182625, Manufactured by STERIS Corporation, 2720…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-0554-2007 |
|---|---|
| Recall event | 37349 |
| Product | Cmax Surgical Table, Model No. 2182625, Manufactured by STERIS Corporation, 2720 Gunter Park East, Montgomery, AL 36109 USA, TEL: 334 277 6660, FAX: 334 271 5450 |
| Product code | GDC |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 11, 2009 |
| FEI number | 1043572 |
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