Device recall
Z-0141-2014: Harmony Equipment Management System, Model #603X/80XX, STERIS Corporation…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-0141-2014 |
|---|---|
| Recall event | 66138 |
| Product | Harmony Equipment Management System, Model #603X/80XX, STERIS Corporation, Mentor, OH Harmony Equipment Management Systems (EMS) are used in hospital facilities to provide ready access to medical gasses, electrical power and audio/visual data services, in addition to managing surgical support… |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2014 |
| FEI number | 1527821 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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