Device recall
Z-1281-2013: Insight Instruments MIS ( Multi-Port Illumination System) Illuminated pilot…
FDA device recall · Class II · Insight Instruments, Inc.
Key facts
| Recall number (Z-number) | Z-1281-2013 |
|---|---|
| Recall event | 64887 |
| Product | Insight Instruments MIS ( Multi-Port Illumination System) Illuminated pilot tubes work like a ceiling light while simultaneously protecting the entry sites. Illumination automatically follows the movement of the two surgical instruments inserted into the M.I.S. cannulas. The large distance of more… |
| Product code | HMX |
| Recalling firm | Insight Instruments, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 21, 2014 |
| FEI number | 1052234 |
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