Device recall
Z-0823-2011: Steris Reliance EPS Endoscope Processing System, manufactured by Corporation…
FDA device recall · Class III · Steris Corporation
Key facts
| Recall number (Z-number) | Z-0823-2011 |
|---|---|
| Recall event | 56245 |
| Product | Steris Reliance EPS Endoscope Processing System , manufactured by Corporation STERIS Canada, Quebec, Canada. Washing and high level disinfection of up to two manually pre-cleaned, immersible, reusable, heat-resistant, semi-critical endoscope devices. |
| Product code | MLR |
| Recalling firm | Steris Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 27, 2012 |
| 510(k) numbers | K040049 |
| 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