Device recall
Z-0154-2016: TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use…
FDA device recall · Class II · Berchtold Corp.
Key facts
| Recall number (Z-number) | Z-0154-2016 |
|---|---|
| Recall event | 72273 |
| Product | TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for use in operating rooms, medical treatment rooms, intensive care units, or any area of a medical facility that requires a ceiling mounted device to supply power, medical gases, and data-communication services. TELETOM is… |
| Product code | FQO |
| Recalling firm | Berchtold Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 17, 2016 |
| FEI number | 1220685 |
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