Device recall
Z-0144-2014: MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25- gauge…
FDA device recall · Class II · Insight Instruments, Inc.
Key facts
| Recall number (Z-number) | Z-0144-2014 |
|---|---|
| Recall event | 66040 |
| Product | MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25- gauge illuminator for vitreo-retinal surgery when full field illumination of bimanual surgery if desired. |
| Product code | HNJ |
| Recalling firm | Insight Instruments, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 27, 2017 |
| FEI number | 1052234 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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